1738-82-5

Basic information

• Product Name: GLY-GLY BENZYL ESTER P-TOLUENESULFONATE SALT
• Synonyms: GLYCYLGLYCINE BENZYL ESTER P-TOLUENESULFONATE;GLYCYLGLYCINE BENZYL ESTER P-TOLUENESULFONATE SALT;GLYCYL-GLYCINE BENZYL ESTER-P-TOSYLATE;GLY-GLY BENZYL ESTER P-TOLUENESULFONATE SALT;H-GLY-GLY-OBZL P-TOSYLATE;H-GLY-GLY-OBZL TOS;H-GLY-GLY-OBZL TOSOH;GLY-GLY BENZYL ESTER P-TOLUENESULFONATE
• CAS NO: 1738-82-5
• Molecular Formula: C₇H₇O₃S*C₁₁H₁₅N₂O₃
• Molecular Weight: 394.44
• Product Categories: Dipeptides;Dipeptides and Tripeptides;Peptides
• Mol File: 1738-82-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 157-159℃
• Boiling Point: 408 °C at 760 mmHg
• Flash Point: 200.5 °C
• Appearance: White powder
• Vapor Pressure: 7.26E-07mmHg at 25°C
• Storage Temp.: 2-8°C
• CAS DataBase Reference: GLY-GLY BENZYL ESTER P-TOLUENESULFONATE SALT(CAS DataBase Reference)
• NIST Chemistry Reference: GLY-GLY BENZYL ESTER P-TOLUENESULFONATE SALT(1738-82-5)
• EPA Substance Registry System: GLY-GLY BENZYL ESTER P-TOLUENESULFONATE SALT(1738-82-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 1738-82-5(Hazardous Substances Data)

Usage

General Description

Gly-Gly benzyl ester p-toluenesulfonate salt is a chemical compound used in the field of biochemistry and pharmaceutical research. It is a derivative of glycine, an amino acid that plays a crucial role in protein synthesis and other biological processes. The benzyl ester p-toluenesulfonate salt form of Gly-Gly is often used as a protective group in peptide synthesis, allowing for selective modification of specific amino acids within a peptide chain. Gly-Gly benzyl ester p-toluenesulfonate salt is commonly used in the production of synthetic peptides for a variety of research and medical applications, and its unique properties make it a valuable tool in the study of proteins and drug development.

InChI:InChI=1/C11H14N2O3.C7H8O3S/c12-6-10(14)13-7-11(15)16-8-9-4-2-1-3-5-9;1-6-2-4-7(5-3-6)11(8,9)10/h1-5H,6-8,12H2,(H,13,14);2-5H,1H3,(H,8,9,10)

Upstream product

• 556-50-3 glycylglycine 
• 104-15-4 toluene-4-sulfonic acid 
• 100-51-6 benzyl alcohol 

Downstream Products

• 2387-23-7 1,3-Dicyclohexylurea 
• 807344-32-7 [2-(3-{[(methylcarbamoylmethyl-carbamoyl)-methyl]-carbamoyl}-propionylamino)-acetylamino]-acetic acid benzyl ester 
• 128404-17-1 [2-((S)-2-{(S)-2-[(S)-6-(2-Benzyloxycarbonylamino-acetylamino)-2-tert-butoxycarbonylamino-hexanoylamino]-3-hydroxy-propionylamino}-4-carbamoyl-butyrylamino)-acetylamino]-acetic acid benzyl ester 
• 128404-16-0 {2-[((S)-1-{(S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-6-tert-butoxycarbonylamino-hexanoylamino]-3-hydroxy-propionyl}-pyrrolidine-2-carbonyl)-amino]-acetylamino}-acetic acid benzyl ester 
• 128404-15-9 N-benzyloxycarbonylglycyl-N^ε-tert-butyloxycarbonyl-lysyl-seryl-glutamyl-glycylglycine benzylester 
• 1616761-77-3 benzyl [[3-(1-nitro-2-phenylethyl)oxetan-3-yl]glycyl]glycinate 
• 1386433-20-0 C₄₆H₅₄N₆O₉S 
• 874306-00-0 C₂₃H₃₀⁽²⁾H₂N₄O₇ 
• 684641-83-6 PGG-OCH₂Ph hydrochloride 
• 874305-95-0 [2-(2-dipropylcarbamoylmethoxy-acetylamino)-acetylamino]-acetic acid benzyl ester 
• 874305-98-3 C₁₈H₂₃⁽²⁾H₂N₃O₆ 

Relevant articles and documents

Fluorescent, synthetic amphiphilic heptapeptide anion transporters: Evidence for self-assembly and membrane localization in liposomes

Synthetic anion transporters (SATs) of the general type (n-C 18H37)2N-COCH2OCH 2CO-(Gly)3-Pro-(Gly)3-O-n-C7H 15, 1, are amphiphilic peptides that form anion

Synthesis, radiolabelling and biological evaluation of terminal oxamide derivatives of mercaptoacetyltriglycine

99mTc-MAG3 is widely used in clinical nuclear medicine as a potential replacement of 131I-OIH for renal function studies. The terminal carbonylglycine in the MAG3 backbone is assumed to be essential for maintain