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METHYL 3,5-DIBROMO-4-METHYLBENZOATE is an organic compound that falls under the category of esters, which are formed from the reaction between carboxylic acids and alcohols. This particular chemical is distinguished by the presence of bromine atoms at the 3 and 5 positions on the benzene ring, along with a methyl group and a benzoate group at the 4th position. Its structural formula is C9H8Br2O2. Although the specific properties and applications of this chemical are not extensively documented, it is likely used in the synthesis of more complex chemicals in the field of chemistry. It may also participate in reactions typical of esters and brominated aromatic compounds. Due to its bromine content, it can cause mild to severe irritation to the skin and eyes and may be harmful if swallowed or inhaled, necessitating proper safety precautions during handling.

74896-66-5

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74896-66-5 Usage

Uses

Used in Chemical Synthesis:
METHYL 3,5-DIBROMO-4-METHYLBENZOATE is used as a chemical intermediate for the synthesis of more complex chemicals in the field of chemistry. Its unique structure with bromine atoms and a benzoate group allows it to be a valuable component in the creation of various organic compounds.
Used in Pharmaceutical Industry:
METHYL 3,5-DIBROMO-4-METHYLBENZOATE is used as a building block in the development of pharmaceutical compounds. Its reactivity and structural features may contribute to the formation of new drug molecules with potential therapeutic applications.
Used in Research and Development:
METHYL 3,5-DIBROMO-4-METHYLBENZOATE is used as a research compound in academic and industrial laboratories. Its properties and reactivity are studied to understand its potential applications and to develop new methods for its synthesis and use in various chemical processes.
Used in Material Science:
METHYL 3,5-DIBROMO-4-METHYLBENZOATE is used as a component in the development of new materials with specific properties. Its unique structure and reactivity may contribute to the creation of materials with improved characteristics for various applications, such as in electronics or coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 74896-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74896-66:
(7*7)+(6*4)+(5*8)+(4*9)+(3*6)+(2*6)+(1*6)=185
185 % 10 = 5
So 74896-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Br2O2/c1-5-7(10)3-6(4-8(5)11)9(12)13-2/h3-4H,1-2H3

74896-66-5 Well-known Company Product Price

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  • Alfa Aesar

  • (B25348)  Methyl 3,5-dibromo-4-methylbenzoate, 98%   

  • 74896-66-5

  • 5g

  • 477.0CNY

  • Detail
  • Alfa Aesar

  • (B25348)  Methyl 3,5-dibromo-4-methylbenzoate, 98%   

  • 74896-66-5

  • 25g

  • 2025.0CNY

  • Detail

74896-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3,5-dibromo-4-methylbenzoate

1.2 Other means of identification

Product number -
Other names METHYL 3,5-DIBROMO-4-METHYLBENZOATE

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:74896-66-5 SDS

74896-66-5Relevant academic research and scientific papers

Preparation method of 3,5-dimethoxy-4-methyl benzoic acid

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Paragraph 0035-0038; 0043-0046, (2021/05/29)

The invention discloses a preparation method of 3,5-dimethoxy-4-methyl benzoic acid, which comprises the following steps: adding methyl 4-methyl benzoate in a first organic solvent, adding bromine, and carrying out bromination reaction to obtain methyl 3,

Process for aromatic ethers

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, (2008/06/13)

A process for the preparation of aromatic ethers by the bromination of a compound of the formula STR1 wherein R1, independently, is hydrogen, hydroxy, lower alkoxy, lower alkyl; m is an integer from 1-4, and A is --CHO, --COOR3 or lower alkyl, and subsequently treating the reaction product of the bromination step with an alkali metal alkoxide in the presence of cuprous halide or oxide, is described.

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