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3543-46-2

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3543-46-2 Usage

General Description

5-Bromo-4-phenylpyrimidine is a chemical compound with the molecular formula C10H7BrN2. It is a heterocyclic organic compound composed of a pyrimidine ring substituted with a bromine atom at the 5-position and a phenyl group at the 4-position. 5-Bromo-4-phenylpyrimidine is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry, for the production of various pharmaceutical drugs and intermediates. Its structure and reactivity make it a versatile tool for the synthesis of a wide range of different compounds, and it is often used as a key intermediate in the development of new pharmaceuticals. Additionally, 5-Bromo-4-phenylpyrimidine is also utilized in research laboratories for the development of new chemical processes and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 3543-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3543-46:
(6*3)+(5*5)+(4*4)+(3*3)+(2*4)+(1*6)=82
82 % 10 = 2
So 3543-46-2 is a valid CAS Registry Number.

3543-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-4-phenylpyrimidine

1.2 Other means of identification

Product number -
Other names 5-bromo-4-phenyl-pyrimidine

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:3543-46-2 SDS

3543-46-2Relevant articles and documents

Metal free C-H functionalization of diazines and related heteroarenes with organoboron species and its application in the synthesis of a CDK inhibitor, meriolin 1

Thatikonda, Thanusha,Singh, Umed,Ambala, Srinivas,Vishwakarma, Ram A.,Singh, Parvinder Pal

, p. 4312 - 4320 (2016/05/24)

Here, we report a metal-free cross-coupling reaction of diazines and related heteroarenes with organoboron species via C-H functionalization. The optimized conditions represent a metal-free method for the activation of aryl/heteroarylboronic acids, which undergo coupling with diazines and related heteroarenes. Optimized conditions also find application in the synthesis of a pyrimidine-based potent CDK inhibitor, meriolin1.

INVESTIGATION OF SOME ELECTROPHILIC REACTIONS OF 4-PHENYL-5-HYDROXYPYRIMIDINE AND ITS 1-OXIDE

Gashev, S. B.,Sedova, V. F.,Smirnov, L. D.,Mamaev, V. P.

, p. 1008 - 1012 (2007/10/02)

A difference in the reactivities of the 2 and 6 positions of the 5-hydroxypyrimidine ring and an effect of the N-oxide group on the direction of electrophilic substitution reactions were demonstrated in the case of synthesized 4-phenyl-5-hydroxypyrimidine and its 1-oxide.

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