17350-66-2

Basic information

• Product Name: N-(Benzyloxycarbonyl)-L-alanine hydrazide
• Synonyms: N-(Benzyloxycarbonyl)-L-alanine hydrazide;N-[(Benzyloxy)carbonyl]-L-alanine hydrazide
• CAS NO: 17350-66-2
• Molecular Formula: C₁₁H₁₅N₃O₃
• Molecular Weight: 0
• Mol File: 17350-66-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(Benzyloxycarbonyl)-L-alanine hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Benzyloxycarbonyl)-L-alanine hydrazide(17350-66-2)
• EPA Substance Registry System: N-(Benzyloxycarbonyl)-L-alanine hydrazide(17350-66-2)

Safety Data

• Hazardous Substances Data: 17350-66-2(Hazardous Substances Data)

Upstream product

• 28819-05-8 (S)-2-benzyloxycarbonylamino-propionic acid methyl ester 
• 60625-90-3 Cbz-alanine ethyl ester 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 79458-92-7 N-(Benzyloxycarbonyl-L-ananyl)-L-histidine 
• 28416-91-3 (S)-benzyl (1-azido-1-oxopropan-2-yl)carbamate 
• 3253-17-6 α-N(L-alanyl)-histidine 
• 287728-93-2 [(S)-1-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester 
• 261729-68-4 1-(Cbz-alanylglycyl)-3,5-dimethylpyrazole 
• 3057-63-4 Cbz-alanylglycylglycine ethyl ester 
• 3057-56-5 Cbz-alanylglycylglycyl hydrazide 
• 58651-28-8 benzyloxycarbonylalanyl-glycine hydrazide 
• 1352815-87-2 C₂₃H₁₉N₃O₅ 
• 1360470-98-9 C₃₆H₃₄N₄O₅S 
• 1360470-86-5 C₂₂H₂₃N₃O₅S 
• 1360470-81-0 Z-Ala-ψ[(C2N2O)SH] 
• 1310714-71-6 Cbz-L-Ala-HdHz 
• 1258792-94-7 C₁₈H₁₇N₃O₃ 

Relevant articles and documents

A favorable, narrow, δh Hansen-parameter domain for gelation of low-molecular-weight amino acid derivatives

In recent years, the design of new low-molecular-weight gelators (LMWGs) has attracted considerable attention because of the interesting supramolecular architectures as well as industrial applications. In this context, the role of the organic solvent in d

Combinatorial synthesis of 3,5-Dimethylene substituted 1,2,4-Triazoles

Combinatorial cyclizations of imidates and hydrazides with methylene linked R groups, generated from the corresponding nitriles and carboxylic acids, respectively, provided a large library of 3,5-dimethylene substituted 1,2,4- trizoles. 2011 Bentham Science Publishers Ltd.

The synthesis of regular copolymers of glycine and alanine.

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