3655-05-8

Basic information

• Product Name: BOC-GLY-ONP
• Synonyms: BOC-GLY-ONP;BOC-GLYCINE 4-NITROPHENYL ESTER;BOC-GLYCINE P-NITROPHENYL ESTER;BOC-GLYCINE-ONP;4-nitrophenyl N-[(1,1-dimethylethoxy)carbonyl]glycinate;N-T-BOC-GLYCINE P-NITROPHENYL ESTERCRYST ALLINE;N-alpha-t-Butyloxycarbonyl-glycine p-nitrophenyl ester;N-(tert-Butoxycarbonyl)glycine 4-nitrophenyl ester
• CAS NO: 3655-05-8
• Molecular Formula: C₁₃H₁₆N₂O₆
• Molecular Weight: 296.28
• EINECS: 222-900-4
• Product Categories: Amino Acid Derivatives
• Mol File: 3655-05-8.mol
• Article Data: 13

Chemical Properties

• Melting Point: 71 °C
• Boiling Point: 457°Cat760mmHg
• Flash Point: 230.2°C
• Appearance: /
• Density: 1.267g/cm³
• Vapor Pressure: 1.54E-08mmHg at 25°C
• Refractive Index: 1.533
• Storage Temp.: 2-8°C
• PKA: 10.65±0.46(Predicted)
• CAS DataBase Reference: BOC-GLY-ONP(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-GLY-ONP(3655-05-8)
• EPA Substance Registry System: BOC-GLY-ONP(3655-05-8)

Safety Data

• WGK Germany: 3
• F: 8
• Hazardous Substances Data: 3655-05-8(Hazardous Substances Data)

Usage

Chemical Properties

Brown powder

Uses

Substrate for chymotrypsin and trypsin.

InChI:InChI=1/C13H16N2O6/c1-13(2,3)21-12(17)14-8-11(16)20-10-6-4-9(5-7-10)15(18)19/h4-7H,8H2,1-3H3,(H,14,17)

Upstream product

• 4530-20-5 BOC-glycine 
• 100-02-7 4-nitro-phenol 
• 13303-10-1 tert-Butyl 4-nitrophenyl carbonate 
• 6000-44-8 sodium glycinate 
• 50780-50-2 4-chloromethoxycarbonyloxy-1-nitrobenzene 
• 42538-64-7 Boc-glycine cesium salt 
• 101623-71-6 iodomethyl(4-nitrophenyl)carbonate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 7647-01-0 hydrogenchloride 
• 107-06-2 1,2-dichloro-ethane 
• 18185-77-8 tert-butyloxycarbonylglycine imidazolide 

Downstream Products

• 75410-01-4 t-butoxycarbonylglycyl-L-glutaminylglycine benzyl ester 
• 140647-57-0 N-(t)-butyloxycarbonyl-glycyl-DL-3,3-difluoro-phenylalanyl methyl ester 
• 100-02-7 4-nitro-phenol 
• 14719-37-0 ethyl 2-(tert-butoxycarbonylamino)acetate 
• 1164-16-5 Z-L-Tyr-OH 
• 64645-55-2 N-(benzyloxycarbonyl)-O-<(tert-butoxycarbonyl)glycyl>-L-tyrosine ethyl ester 
• 65853-69-2 N-BOC-glycyl-O-benzyl-L-tyrosin-ethylester 
• 131453-24-2 Boc-Gly-Gln-Cys(MBzl)-Thr-OMe 
• 131453-12-8 Boc-Gly-Cys(MBzl)-Gly-Lys(Z)-OBzl 
• 107326-96-5 Boc-Gly-Trp-Lys(Z)-OCH₃ 
• 4530-20-5 BOC-glycine 
• 35150-09-5 N-(tert-butoxycarbonyl)glycine 
• 17639-39-3 p-nitrophenyl glycinate 
• 73994-88-4 Boc-Gly-Phe-Leu-OBzl 

Relevant articles and documents

Kilogram-Scale Synthesis of Osteogenic Growth Peptide (10-14) Using a Fragment Coupling Approach

Kilogram-scale synthesis of a bioactive pentapeptide in solution by "3 + 2" fragment coupling strategy has been successively accomplished in the development of OGP (10-14), a minimal OGP-derived sequence that retains the full proliferative activity of the osteogenic growth peptide. The synthetic scheme, coupling conditions, and scaling-up of the process are systematically studied; the epimerization of the tripeptide fragment and pentapeptide are also evaluated.

Pesticidal compositions and processes related thereto

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula ("Formula One"): and processes associated therewith.