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1032350-07-4

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1032350-07-4 Usage

General Description

4-Amino-2-chloronicotinaldehyde 2,2,2-trifluoroacetate is a chemical compound with potential pharmaceutical applications. It contains a 4-amino-2-chloronicotinaldehyde core attached to a 2,2,2-trifluoroacetate moiety. 4-Amino-2-chloronicotinaldehyde 2,2,2-trifluoroacetate has been studied for its potential use in the development of new drugs, particularly in the field of medicine. Its properties and structure make it a promising candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1032350-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,3,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1032350-07:
(9*1)+(8*0)+(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*0)+(1*7)=84
84 % 10 = 4
So 1032350-07-4 is a valid CAS Registry Number.

1032350-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-2-chloropyridine-3-carbaldehyde,2,2,2-trifluoroacetic acid

1.2 Other means of identification

Product number -
Other names 4-Amino-2-chloronicotinaldehyde 2,2,2-trifluoroacetate

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:1032350-07-4 SDS

1032350-07-4Relevant articles and documents

Inhibitors of Akt activity

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Page/Page column 60, (2008/12/06)

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt activity by administering the compound to a patient in need of treatment of cancer.

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