98035-61-1

Basic information

• Product Name: H-VAL-GLY-NH2 HCL
• Synonyms: H-VAL-GLY-NH2 HCL;H-Val-Gly-NH2 hydrochloride;Val-Gly-NH2·HCl≥ 95% (HPLC)
• CAS NO: 98035-61-1
• Molecular Formula: C₇H₁₅N₃O₂
• Molecular Weight: 209.67
• Mol File: 98035-61-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: -15°C
• CAS DataBase Reference: H-VAL-GLY-NH2 HCL(CAS DataBase Reference)
• NIST Chemistry Reference: H-VAL-GLY-NH2 HCL(98035-61-1)
• EPA Substance Registry System: H-VAL-GLY-NH2 HCL(98035-61-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 98035-61-1(Hazardous Substances Data)

Usage

Chemical Properties

White to off-white powder

Upstream product

• 871878-30-7 N-(α-bromo-isovaleryl)-glycine amide 
• 26464-05-1 2-bromo-3-methyl-butyryl bromide 
• 33477-43-9 Z-L-valylglycinamide 
• 165900-96-9 Boc-Val-Gly-NH₂ 
• 3392-12-9 Boc-Val-ONSu 
• 3496-11-5 2,5-dioxopyrrolidin-1-yl (2S)-2-(((benzyloxy)carbonyl)amino)-3-methylbutanoate 

Downstream Products

• 147424-36-0 Z-Val-Val-Gly-NH₂ 
• 147424-40-6 Z-Asp(OtBu)-Val-Gly-NH₂ 
• 165901-00-8 H-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 147424-44-0 Boc-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-03-1 H-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-06-4 H-D-Ala-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-02-0 Boc-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-05-3 Boc-D-Ala-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-08-6 Z-Tyr-D-Ala-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 165901-09-7 Z-Tyr(SO₃H)-D-Ala-Phe-Asp(OBzl)-Val-Val-Gly-NH₂ 
• 132125-58-7 H-Tyr-D-Ala-Phe-Val-Asp-Val-Gly-NH₂ 
• 122752-15-2 deltorphin C 
• 147424-50-8 Z-Val-Asp(OtBu)-Val-Gly-NH₂ 
• 147424-43-9 Z-Asp(OtBu)-Val-Val-Gly-NH₂ 

Relevant articles and documents

2,2-Dimethyl-2-(o-nitrophenyl)acetyl (DMNA) as an assisted cleavage protecting group for amines

2,2-Dimethyl-2-(o-nitrophenyl)acetyl group (DMNA) was explored as an assisted cleavage protecting group for amines and a one-step deprotection condition was developed for its efficient removal using hydrogenation in the presence of Pd-C or PtO2 catalyst and 10% HOAc in MeOH. DMNA was found to be especially useful for the synthesis of gem-diamino compounds using Hofmann rearrangement.

Unique sequence in deltorphin C confers structural requirement for δ opioid receptor selectivity

A series of deltorphin C (H-Tyr-D-Ala-Phe-Asp-Val-Val-Gly-NH2) analogues were synthesized to assess the consequences of changing anionic and hydrophobic residues on δ receptor selectivity.Analogues with altered C-terminal groups, inverted sequences, or es