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6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER is a chemical compound characterized by the molecular formula C9H7BrNO3. It is a methyl ester derivative of benzooxazole-2-carboxylic acid, featuring a bromine atom that contributes to its unique chemical properties. This versatile compound is widely recognized for its potential in the synthesis of pharmaceuticals and agrochemicals, as well as its applications in medicinal chemistry research and the development of new drug candidates.

954239-67-9

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954239-67-9 Usage

Uses

Used in Pharmaceutical Industry:
6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drug candidates. Its unique structure and properties make it a valuable component in the creation of innovative medications.
Used in Agrochemical Industry:
In the agrochemical sector, 6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER serves as an intermediate in the synthesis of agrochemicals, playing a crucial role in the development of new compounds for agricultural applications, such as pesticides and herbicides.
Used in Medicinal Chemistry Research:
6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER is utilized as a key component in medicinal chemistry research, where it aids in the exploration and advancement of novel therapeutic agents. Its unique chemical structure allows for the design and synthesis of potential drug candidates with improved efficacy and selectivity.
Used in Organic Synthesis:
6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER is employed in the field of organic synthesis, where it contributes to the creation of a wide range of chemical compounds. Its versatility and reactivity make it a valuable building block for the synthesis of various organic molecules.
Used in Chemical Manufacturing:
In the chemical manufacturing industry, 6-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER is used as a versatile compound with potential applications in the production of various chemical products. Its unique properties and reactivity make it a valuable asset in the development of new chemical processes and products.

Check Digit Verification of cas no

The CAS Registry Mumber 954239-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,2,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 954239-67:
(8*9)+(7*5)+(6*4)+(5*2)+(4*3)+(3*9)+(2*6)+(1*7)=199
199 % 10 = 9
So 954239-67-9 is a valid CAS Registry Number.

954239-67-9SDS

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 Methyl 6-bromobenzo[d]oxazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 6-bromo-1,3-benzoxazole-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:954239-67-9 SDS

954239-67-9Downstream Products

954239-67-9Relevant academic research and scientific papers

Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide

Chen, Jing-Huo,Deng, Cheng-Hua,Fang, Sheng,Ma, Jian-Gong,Cheng, Peng

, p. 989 - 996 (2018)

The triply bonded dimolybdenum compound, Mo2(OtBu)6 (1), was investigated as a homogeneous catalyst for the conversion of CO2. The compound 1 acted as a rare example of a versatile catalyst with an impressive ability to transform CO2 into various valuable products, including propiolic acids, cyclic carbonates, and benzo[d]thiazole- and benzo[d]oxazolecarboxylic acids, in high yields with short reaction times and excellent selectivity at ambient pressure and low temperatures (25-75 °C). This is the first report of the application of a metal-metal bond-containing species in the catalytic conversion of CO2.

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