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3921-01-5

3921-01-5

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3921-01-5 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 3921-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3921-01:
(6*3)+(5*9)+(4*2)+(3*1)+(2*0)+(1*1)=75
75 % 10 = 5
So 3921-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Br2N2/c5-3-1-2-7-4(6)8-3/h1-2H

3921-01-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H27433)  2,4-Dibromopyrimidine, 95%   

  • 3921-01-5

  • 1g

  • 3391.0CNY

  • Detail

  • Alfa Aesar

  • (H27433)  2,4-Dibromopyrimidine, 95%   

  • 3921-01-5

  • 5g

  • 7820.0CNY

  • Detail

3921-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dibromopyrimidine

1.2 Other means of identification

Product number -
Other names 2,4-dibromopyrimidine

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:3921-01-5 SDS

3921-01-5Relevant articles and documents

Syntheses of various 5-(bromoaryl)-substituted uracils

Wellmar,Hornfeldt,Gronowitz

, p. 1159 - 1163 (1995)

The Suzuki Pd(0)-catalyzed coupling between arylboronic acids and aryl bromides or iodides in weakly alkaline medium, previously further developed by us, has been used for regioselective preparation of 5-(2'-bromo-5'-furyl)-, 5-(2'-bromo-4'-furyl)-, 5-(2'

Regio- and chemoselective multiple functionalization of pyrimidine derivatives by selective magnesiations using TMPMgCl·LiCl

Mosrin, Marc,Knochel, Paul

supporting information; experimental part, p. 2497 - 2500 (2009/05/30)

(Chemical Equation Presented) Successive regio- and chemoselective magnesiations of pyrimidines using TMPMgCl·LiCl furnish, after trapping with various electrophiles, highly functionalized derivatives in good to excellent yields. Applications to the synth

Arylation of halogenated pyrimidines via a suzuki coupling reaction

Schomaker,Delia

, p. 7125 - 7128 (2007/10/03)

The Suzuki coupling reaction has been used extensively for the synthesis of a wide variety of unsymmetrical biaryl compounds. We have extended this reaction to demonstrate the utility of preparing monophenyl-, diphenyl-, or triphenylpyrimidine depending on the reaction conditions. Further, it has been shown that chloropyrimidine substrates are preferable over iodo-, bromo-, or fluoropyrimidines.

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