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815610-16-3

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815610-16-3 Usage

General Description

4-Iodopyrimidin-2-amine, also known as 2-amino-4-iodopyrimidine, is a chemical compound with the molecular formula C4H4IN3. It is a halogenated derivative of pyrimidine and contains an amino group. 4-Iodopyrimidin-2-amine is commonly used in the synthesis of pharmaceuticals and is used as a building block in the preparation of various bioactive molecules. Its combination of an amine and iodine group make it a versatile intermediate for organic synthesis, allowing for the creation of a wide range of novel compounds for medicinal and scientific research.

Check Digit Verification of cas no

The CAS Registry Mumber 815610-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,5,6,1 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 815610-16:
(8*8)+(7*1)+(6*5)+(5*6)+(4*1)+(3*0)+(2*1)+(1*6)=143
143 % 10 = 3
So 815610-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H4IN3/c5-3-1-2-7-4(6)8-3/h1-2H,(H2,6,7,8)

815610-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-iodopyrimidine

1.2 Other means of identification

Product number -
Other names 4-Iodopyrimidin-2-amine

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:815610-16-3 SDS

815610-16-3Upstream product

815610-16-3Relevant articles and documents

Synthesis and structure-activity relationship of trisubstituted thiazoles as Cdc7 kinase inhibitors

Reichelt, Andreas,Bailis, Julie M.,Bartberger, Michael D.,Yao, Guomin,Shu, Hong,Kaller, Matthew R.,Allen, John G.,Weidner, Margaret F.,Keegan, Kathleen S.,Dao, Jennifer H.

, p. 364 - 382 (2014/05/20)

The Cell division cycle 7 (Cdc7) protein kinase is essential for DNA replication and maintenance of genome stability. We systematically explored thiazole-based compounds as inhibitors of Cdc7 kinase activity in cancer cells. Our studies resulted in the identification of a potent, selective Cdc7 inhibitor that decreased phosphorylation of the direct substrate MCM2 in vitro and in vivo, and inhibited DNA synthesis and cell viability in vitro.

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