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191729-21-2

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191729-21-2 Usage

General Description

2-Chloro-4-(phenylthio)pyrimidine is a chemical compound with the molecular formula C10H7ClN2S. It is a pyrimidine derivative that contains a chlorine atom and a phenylthio group (C6H5S) attached to the pyrimidine ring. 2-CHLORO-4-(PHENYLTHIO)PYRIMIDINE is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it can also be used as a building block for the preparation of various other functionalized pyrimidine derivatives. Its versatile reactivity and potential as a key building block in organic synthesis make it a valuable compound in the field of medicinal and agricultural chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 191729-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,7,2 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191729-21:
(8*1)+(7*9)+(6*1)+(5*7)+(4*2)+(3*9)+(2*2)+(1*1)=152
152 % 10 = 2
So 191729-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H7ClN2S/c11-10-12-7-6-9(13-10)14-8-4-2-1-3-5-8/h1-7H

191729-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-phenylsulfanylpyrimidine

1.2 Other means of identification

Product number -
Other names 2-chloro-4-phenyl-sulphanylpyrimidine

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:191729-21-2 SDS

191729-21-2Relevant articles and documents

HFIP Promoted Low-Temperature SNAr of Chloroheteroarenes Using Thiols and Amines

Bhujabal, Yuvraj B.,Vadagaonkar, Kamlesh S.,Gholap, Aniket,Sanghvi, Yogesh S.,Dandela, Rambabu,Kapdi, Anant R.

, p. 15343 - 15354 (2019/12/04)

A highly efficient and an unprecedented hexafluoro-2-propanol, promoting low-temperature aromatic nucleophilic substitutions of chloroheteroarenes, has been performed using thiols and (secondary) amines under base-free and metal-free conditions. The developed protocol also provides excellent regio-control for the selective functionalization of dichloroheteroarenes, while the utility of the protocol was demonstrated by the modification of a commercially available drug ceritinib.

SUBSTITUTED 2-ANILINOPYRIMIDINES USEFUL AS PROTEIN KINASE INHIBITORS

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, (2008/06/13)

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