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574729-41-2

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574729-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 574729-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,4,7,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 574729-41:
(8*5)+(7*7)+(6*4)+(5*7)+(4*2)+(3*9)+(2*4)+(1*1)=192
192 % 10 = 2
So 574729-41-2 is a valid CAS Registry Number.

574729-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butoxycarbonylamino-2-(3,4-dichloro-phenyl)-butyric acid

1.2 Other means of identification

Product number -
Other names 4-tert-butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric 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:574729-41-2 SDS

574729-41-2Relevant academic research and scientific papers

AKT PROTEIN KINASE INHIBITORS

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Page/Page column 134-135; 105-106, (2008/06/13)

The present invention provides compounds, including resolved enantiomers, diastereomers, solvates and pharmaceutically acceptable salts thereof, comprising the Formula: A-L-CR where CR is a cyclical core group, L is a linking group and A is as defined herein. Also provided are methods of using the compounds of this invention as AKT protein kinase inhibitors and for the treatment of hyperproliferative diseases such as cancer.

Indazole compounds useful as protein kinase inhibitors

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, (2008/06/13)

The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein R1, R2, V1, V2, and V3 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of AKT, PKA, PDK1, p70S6K, or ROCK kinase, mammalian protein kinases involved in proliferative and neurodegenerative disorders. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of utilizing those compositions in the treatment of various disorders.

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