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913739-29-4

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913739-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913739-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,7,3 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 913739-29:
(8*9)+(7*1)+(6*3)+(5*7)+(4*3)+(3*9)+(2*2)+(1*9)=184
184 % 10 = 4
So 913739-29-4 is a valid CAS Registry Number.

913739-29-4SDS

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 tert-butyl (3-amino-1-phenyl-1H-pyrazol-4-yl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 3-amino-1-phenyl-1H-pyrazol-4-ylcarbamate

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:913739-29-4 SDS

913739-29-4Relevant articles and documents

PHOSPHORUS DERIVATIVES AS HISTONE DEACETYLASE INHIBITORS

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Page/Page column 134, (2008/06/13)

The present invention relates to a novel class of phosphorus derivatives. The phosphorus compounds can be used to treat cancer. The phosphorus compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differe

FLUORINATED ARYLAMIDE DERIVATIVES

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Page/Page column 60, (2008/06/13)

The present invention relates to a novel class of fluorinated arylamide derivatives. The instant compounds can be used to treat cancer. The fluorinated arylamide derivatives can also inhibit histone deacetylase and are suitable for use in selectively indu

Spirocyclic compounds

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Page/Page column 30, (2008/06/13)

The present invention relates to a novel class of substituted spirocyclic compounds. These compounds can inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of n

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