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methyl 3-amino-3-(2-methoxyphenyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1009289-77-3

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1009289-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1009289-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,2,8 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1009289-77:
(9*1)+(8*0)+(7*0)+(6*9)+(5*2)+(4*8)+(3*9)+(2*7)+(1*7)=153
153 % 10 = 3
So 1009289-77-3 is a valid CAS Registry Number.

1009289-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-amino-3-(2-methoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names METHYL3-AMINO-3-(2-METHOXYPHENYL)PROPANOATE

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:1009289-77-3 SDS

1009289-77-3Relevant academic research and scientific papers

Synthesis, in vitro and in vivo biological evaluation, and comprehensive understanding of structure-activity relationships of dipeptidyl boronic acid proteasome inhibitors constructed from β-amino acids

Zhu, Yongqiang,Wu, Gang,Zhu, Xinrong,Ma, Yuheng,Zhao, Xin,Li, Yuejie,Yuan, Yunxia,Yang, Jie,Yu, Sen,Shao, Feng,Lei, Meng

supporting information; experimental part, p. 8619 - 8626 (2011/03/20)

An extensive structure-activity relationship (SAR) study of 72 dipeptidyl boronic acid proteasome inhibitors constructed fromβ -amino acids is reported. SAR analysis revealed that bicyclic groups at the R1 position, 3-F substituents at the Rsu

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