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Gugus aminometil - Riwayat revisi
2026-09-16T01:37:19Z
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Maintenance script: Presentation V4: sitasi, referensi, Math, Wikimedia Commons, dan atribusi
2026-08-29T09:16:12Z
<p>Presentation V4: sitasi, referensi, Math, Wikimedia Commons, dan atribusi</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Revisi sebelumnya</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revisi per 29 Agustus 2026 09.16</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l4">Baris 4:</td>
<td colspan="2" class="diff-lineno">Baris 4:</td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Biasanya gugus aminometil memiliki amina tersier. Seringkali gugus ini diperoleh melalui alkilasi dengan garam Eschenmoser, sumber [CH<sub>2</sub>=N(CH<sub>3</sub>)<sub>2</sub>]<sup>+</sup>.</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Biasanya gugus aminometil memiliki amina tersier. Seringkali gugus ini diperoleh melalui alkilasi dengan garam Eschenmoser, sumber [CH<sub>2</sub>=N(CH<sub>3</sub>)<sub>2</sub>]<sup>+</sup>.</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Kompleks kobalt(III) dari aminometil dikenal dalam bentuk [Ko([[bipiridina]])<sub>2</sub>(CH<sub>2</sub>NH<sub>2</sub>)](ClO<sup>4</sup>)<sub>2</sub>.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Kompleks kobalt(III) dari aminometil dikenal dalam bentuk [Ko([[bipiridina]])<sub>2</sub>(CH<sub>2</sub>NH<sub>2</sub>)](ClO<sup>4</sup>)<sub>2</sub>.<ins style="font-weight: bold; text-decoration: none;"><ref>A. L. Poznyak. ''New Type of Organocobalt Complexes Structure of η 2 -aminomethylenebis(2,2?-bipyridyl) Cobalt(III)''. ''Monatshefte fuer Chemie''. 1982. Vol. 113 (5). hlm. 561–564. doi:10.1007/BF00800262.</ref></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Aminometil adalah anggota pertama dari serangkaian gugus 1-aminoalkil dengan bentuk .</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Aminometil adalah anggota pertama dari serangkaian gugus 1-aminoalkil dengan bentuk .<ins style="font-weight: bold; text-decoration: none;"><ref>Erwin Von Angerer, Norbert Knebel, Mario Kager, and Bernhard Ganss </ins>(<ins style="font-weight: bold; text-decoration: none;">1990</ins>)<ins style="font-weight: bold; text-decoration: none;">: "1</ins>-(<ins style="font-weight: bold; text-decoration: none;">aminoalkyl</ins>)<ins style="font-weight: bold; text-decoration: none;">-2-phenylindoles as novel pure estrogen antagonists". ''Journal of Medicinal Chemistry'', volume 33, issue 9, pages 2635–2640</ins>.<ins style="font-weight: bold; text-decoration: none;"></ref></ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div> </div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">Aminometil digunakan dalam nama standar </del>(<del style="font-weight: bold; text-decoration: none;">[[Persatuan Kimia Murni dan Terapan Internasional|IUPAC]]</del>) <del style="font-weight: bold; text-decoration: none;">beberapa senyawa seperti asam 4</del>-(<del style="font-weight: bold; text-decoration: none;">aminometil</del>)<del style="font-weight: bold; text-decoration: none;">benzoat</del>.</div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div> </div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">==Referensi==</del></div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Aminometil digunakan dalam nama standar ([[Persatuan Kimia Murni dan Terapan Internasional|IUPAC]]) beberapa senyawa<ref>Ursula Bünzli-Trepp (2007): ''Systematic Nomenclature of Organic, Organometallic and Coordination Chemistry: Chemical-Abstracts Guidelines with IUPAC Recommendations and Many Trivial Names''. EPFL Press, 636 pages.</ref> seperti asam 4-(aminometil)benzoat.</ins></div></td></tr>
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<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">== Referensi ==</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"><references /></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Sumber dan atribusi ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Sumber dan atribusi ==</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Gugus+aminometil&oldid=29061387 Wikipedia bahasa Indonesia], revisi 29061387 (2026-03-23T05:19:57Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Gugus+aminometil&oldid=29061387 Wikipedia bahasa Indonesia], revisi 29061387 (2026-03-23T05:19:57Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</div></td></tr>
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2026-08-29T08:55:03Z
<p>Impor teks terkontrol dari Wikipedia bahasa Indonesia; revisi 29061387; atribusi sumber disertakan.</p>
<p><b>Halaman baru</b></p><div>Dalam [[kimia organik]], '''gugus aminometil''' adalah [[gugus fungsi]]onal [[valensi|monovalen]] dengan [[rumus kimia]] . Gugus ini dapat digambarkan sebagai [[gugus metil]] yang disubstitusi oleh gugus amino .<br />
<br />
==Senyawa terkait==<br />
Biasanya gugus aminometil memiliki amina tersier. Seringkali gugus ini diperoleh melalui alkilasi dengan garam Eschenmoser, sumber [CH<sub>2</sub>=N(CH<sub>3</sub>)<sub>2</sub>]<sup>+</sup>.<br />
<br />
Kompleks kobalt(III) dari aminometil dikenal dalam bentuk [Ko([[bipiridina]])<sub>2</sub>(CH<sub>2</sub>NH<sub>2</sub>)](ClO<sup>4</sup>)<sub>2</sub>.<br />
<br />
Aminometil adalah anggota pertama dari serangkaian gugus 1-aminoalkil dengan bentuk .<br />
<br />
Aminometil digunakan dalam nama standar ([[Persatuan Kimia Murni dan Terapan Internasional|IUPAC]]) beberapa senyawa seperti asam 4-(aminometil)benzoat.<br />
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==Referensi==<br />
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== Sumber dan atribusi ==<br />
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Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Gugus+aminometil&oldid=29061387 Wikipedia bahasa Indonesia], revisi 29061387 (2026-03-23T05:19:57Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</div>
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