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C(CN)C(=O)N製品情報
3-aminopropanamide (CAS 4726-85-6) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 192802
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5fe80e28be3a4927bfcee9882cecc52b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2be33ee2af674913aabb220a141fef41反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-7e2ddbc6f04840c0a7f58d3e0a9f47e4反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Compound 73 was prepared according to the procedure described for the synthesis of compound 72 by replacing leucine amide with 3-aminopropanamide. LCMS (+ESI) m/z=495.4 [M+H]+.
ソース ID: ord-ffc49bd9bd9b49a5a5b5829d85ea1b93反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Compound 73 was prepared according to the procedure described for the synthesis of compound 72 by replacing leucine amide with 3-aminopropanamide. LCMS (+ESI) m/z=495.4 [M+H]+.
ソース ID: ord-ffc49bd9bd9b49a5a5b5829d85ea1b93反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The title compound was prepared in analogy to Example 52, from 3-{2,5-dichloro-4-[3-(4-cyclopropyl-3,4-dihydro-2H-quinoxaline-1-carbonyl)-pyridin-4-yloxy]-benzoylamino}-propionic acid (Example 34) and 3-amino-propionamide (commercially available, CAS RN 4726-85-6). Light brown foam (74%). MS (ESI): m/z=554.136 [M+H]+.
ソース ID: ord-6de6306c5aa64bcb96316f600d76e736反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The title compound was prepared in analogy to Example 52, from 3-{2,5-dichloro-4-[3-(4-cyclopropyl-3,4-dihydro-2H-quinoxaline-1-carbonyl)-pyridin-4-yloxy]-benzoylamino}-propionic acid (Example 34) and 3-amino-propionamide (commercially available, CAS RN 4726-85-6). Light brown foam (74%). MS (ESI): m/z=554.136 [M+H]+.
ソース ID: ord-6de6306c5aa64bcb96316f600d76e736反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: CyanoAla, Thio-Asn, Asp, Gln, Glu, β-Ala-NH2, D-Asn, Asn-NH2
ソース ID: ord-92f992bbe8064152a9b6944067269739反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Compound 73 was prepared according to the procedure described for the synthesis of compound 72 by replacing leucine amide with 3-aminopropanamide. LCMS (+ESI) m/z=495.4 [M+H]+.
ソース ID: ord-ffc49bd9bd9b49a5a5b5829d85ea1b93反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5fe80e28be3a4927bfcee9882cecc52b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2be33ee2af674913aabb220a141fef41反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-7e2ddbc6f04840c0a7f58d3e0a9f47e4PubChem References
化合物の公開データベース記録に掲載された情報源です。
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