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62880-67-5

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62880-67-5 Usage

General Description

5-Bromo-2-chloro-4-(1-piperidinyl)pyrimidine is a chemical compound with the molecular formula C10H10BrClN3. It is a pyrimidine derivative and is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 5-BROMO-2-CHLORO-4-(1-PIPERIDINYL)PYRIMIDINE is known for its potential biological activity, and it has been studied for its use in the development of new drugs. It has also been used in research as a precursor for the synthesis of various heterocyclic compounds. Additionally, it is known for its applications in the field of medicinal chemistry and drug discovery. Overall, 5-Bromo-2-chloro-4-(1-piperidinyl)pyrimidine is a versatile chemical compound with diverse applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 62880-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,8 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62880-67:
(7*6)+(6*2)+(5*8)+(4*8)+(3*0)+(2*6)+(1*7)=145
145 % 10 = 5
So 62880-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11BrClN3/c10-7-6-12-9(11)13-8(7)14-4-2-1-3-5-14/h6H,1-5H2

62880-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-2-chloro-4-piperidin-1-ylpyrimidine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:62880-67-5 SDS

62880-67-5Relevant articles and documents

Synthesis of trisubstituted pyrimidines by regioselective SNAr and Suzuki reactions of polyhalopyrimidines

Large, Jonathan M.,Clarke, Maria,Williamson, David M.,McDonald, Edward,Collins, Ian

, p. 861 - 864 (2007/10/03)

An efficient, regioselective approach to the synthesis of trisubstituted pyrimidines was developed. Sequential functionalisation of commercially available polyhalopyrimidines provided the target compounds in moderate to good overall yields. Georg Thieme V

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