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ETHYL 3-BROMOIMIDAZO[1,2-A]PYRIMIDINE-2-CARBOXYLATE is a chemical compound that belongs to the family of imidazopyrimidines, which are organic compounds containing an imidazo ring fused to a pyrimidine ring. As a bromide compound, it has the bromine atom connected to the carbon atoms on the imidazo[1,2-a]pyrimidine ring. ETHYL 3-BROMOIMIDAZO[1,2-A]PYRIMIDINE-2-CARBOXYLATE also contains an ethoxy group and a carboxylate group, which contribute to its chemical properties. Specific details about its application, toxicity, and handling precautions might vary and are crucial to be obtained from reliable sources or material safety data sheets.

134044-63-6

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134044-63-6 Usage

Uses

ETHYL 3-BROMOIMIDAZO[1,2-A]PYRIMIDINE-2-CARBOXYLATE is used as a chemical intermediate for the synthesis of various compounds in the pharmaceutical and chemical industries. Its unique structure and functional groups make it a valuable building block for the development of new drugs and materials. However, the specific applications and reasons for its use may vary depending on the industry and the intended purpose. It is essential to consult reliable sources or material safety data sheets for detailed information on its applications, toxicity, and handling precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 134044-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,4 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134044-63:
(8*1)+(7*3)+(6*4)+(5*0)+(4*4)+(3*4)+(2*6)+(1*3)=96
96 % 10 = 6
So 134044-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrN3O2/c1-2-15-8(14)6-7(10)13-5-3-4-11-9(13)12-6/h3-5H,2H2,1H3

134044-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-bromoimidazo[1,2-a]pyrimidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 3-BROMOIMIDAZO[1,2-A]PYRIMIDINE-2-CARBOXYLATE

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:134044-63-6 SDS

134044-63-6Downstream Products

134044-63-6Relevant academic research and scientific papers

A quick, mild and efficient bromination using a CFBSA/KBr system

Jiang, Pan-Pan,Yang, Xian-Jin

, p. 90031 - 90034 (2016/10/09)

Bromination is a fundamental transformation in organic chemistry and brominated compounds as building blocks are of paramount importance in organic synthesis. In our study, we have developed an efficient method of bromination by using a CFBSA/KBr system at room temperature in a short reaction time. Notably, this approach has been proven to be applicable to a range of substrates including 1,3-diketones and β-keto esters, phenols, aromatic amines and heteroarenes with good to excellent yields.

Antifungal activity in vitro of some imidazopyrimidine derivatives

Rival, Y,Grassy, G,Taudou, A,Ecalle, R

, p. 13 - 18 (2007/10/02)

In regard to fungicidal activity of imidazole ring found in chemical compounds such as econazole, a series of 42 diversely substituted imidazopyrimidines was synthetized and examined for its antifungal activity in several species.

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