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947661-79-2

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947661-79-2 Usage

General Description

4-[tert-butoxycarbonyl-[(4-methoxyphenyl)methyl]amino]butanoic acid is a chemical compound with potential applications in pharmaceutical and medicinal chemistry. It is a derivative of the amino acid butanoic acid, and its structure includes a tert-butoxycarbonyl group and a 4-methoxyphenylmethylamino group. 4-[tert-butoxycarbonyl-[(4-methoxyphenyl)methyl]amino]butanoic acid is of interest due to its potential as a drug precursor or intermediate, as well as its ability to modify the properties and functions of peptides. Its structure suggests that it may be used in the synthesis of peptide-based drugs or in the development of new therapeutic agents. Additionally, the presence of a methoxy group in its structure may confer unique pharmacological properties, making it a valuable chemical for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 947661-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,6,6 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 947661-79:
(8*9)+(7*4)+(6*7)+(5*6)+(4*6)+(3*1)+(2*7)+(1*9)=222
222 % 10 = 2
So 947661-79-2 is a valid CAS Registry Number.

947661-79-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-methoxyphenyl)methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(tert-Butoxycarbonyl(4-methoxybenzyl)amino)butanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:947661-79-2 SDS

947661-79-2Relevant articles and documents

Design and synthesis of novel pyrimido[4,5-b]azepine derivatives as HER2/EGFR dual inhibitors

Kawakita, Youichi,Seto, Masaki,Ohashi, Tomohiro,Tamura, Toshiya,Yusa, Tadashi,Miki, Hiroshi,Iwata, Hidehisa,Kamiguchi, Hidenori,Tanaka, Toshimasa,Sogabe, Satoshi,Ohta, Yoshikazu,Ishikawa, Tomoyasu

, p. 2250 - 2261 (2013/05/09)

A novel 7,6 fused bicyclic scaffold, pyrimido[4,5-b]azepine was designed to fit into the ATP binding site of the HER2/EGFR proteins. The synthesis of this scaffold was accomplished by an intramolecular Claisen-type condensation. As the results of optimiza

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