79722-09-1

Basic information

• Product Name: N-BOC-L-ALA-NHOBN
• Synonyms: N-BOC-L-ALA-NHOBN
• CAS NO: 79722-09-1
• Molecular Formula: C₁₅H₂₂N₂O₄
• Molecular Weight: 294.35
• Product Categories: pharmacetical
• Mol File: 79722-09-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.119g/cm³
• Refractive Index: 1.512
• CAS DataBase Reference: N-BOC-L-ALA-NHOBN(CAS DataBase Reference)
• NIST Chemistry Reference: N-BOC-L-ALA-NHOBN(79722-09-1)
• EPA Substance Registry System: N-BOC-L-ALA-NHOBN(79722-09-1)

Safety Data

• Hazardous Substances Data: 79722-09-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H22N2O4/c1-11(16-14(19)21-15(2,3)4)13(18)17-20-10-12-8-6-5-7-9-12/h5-9,11H,10H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1

Upstream product

• 15761-38-3 L-N-Boc-Ala 
• 622-33-3 N-benzyloxyamine 
• 28875-17-4 (S)-N-(tert-butoxycarbonyl)alanine methyl ester 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 

Downstream Products

• 123984-19-0 (S)-Pyrrolidine-2-carboxylic acid [1-((S)-1-benzyloxycarbamoyl-ethylcarbamoyl)-3-methyl-butyl]-amide; hydrochloride 
• 123984-19-0 HCl*Pro-Leu-Ala-NHOBzl 
• 123984-20-3 (S)-1-Benzoyl-pyrrolidine-2-carboxylic acid [1-((S)-1-benzyloxycarbamoyl-ethylcarbamoyl)-3-methyl-butyl]-amide 
• 123984-20-3 Bz-Pro-Leu-Ala-NHOBzl 
• 123984-18-9 (S)-2-[1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-3-methyl-butylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 123984-18-9 (S)-2-[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-3-methyl-butylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 123984-16-7 [1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-3-methyl-butyl]-carbamic acid tert-butyl ester 
• 123984-16-7 Boc-Leu-Ala-NHOBzl 
• 129585-32-6 (S)-1-Benzoyl-pyrrolidine-2-carboxylic acid [(S)-1-((S)-1-benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethyl]-amide 
• 123984-23-6 (S)-2-[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 123984-22-5 [(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester 
• 79722-20-6 O-benzyl N-methyl-N^α-(tert-butoxycarbonyl)-N^α-methyl-L-alaninehydroxamate 
• 79735-23-2 O-benzyl N^α-(tert-butoxycarbonyl)-N^α-methyl-L-alaninehydroxamate 
• 79722-14-8 O-benzyl N-methyl-N^α-(tert-butoxycarbonyl)-L-alaninehydroxamate 

Relevant articles and documents

Synthesis of O-benzyl hydroxamates employing the sulfonate esters of N-hydroxybenzotriazole

The direct conversion of various carboxylic acids, that include sterically hindered amino acids and di-peptides, to O-benzyl hydroxamates is demonstrated using sulfonate esters of benzotriazoles under ambient and milder conditions without significant race

Design, synthesis and utilization of a novel coupling reagent for the preparation of O-alkyl hydroxamic acids

An efficient novel reagent, phosphoric acid diethyl ester 2-phenyl-benzimidazol-1-yl ester, was designed, and synthesized and its applicability was demonstrated for the preparation of O-alkyl hydroxamic acids. The O-alkyl hydroxamic acids of N-protected a

N-Methylation of O-Benzyl Nα-(Alkoxycarbonyl)α-Amino Acid Hydroxamate Derivatives

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