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3,5-DIBROMO-4-METHYLBENZOIC ACID is a chemical compound characterized by the molecular formula C8H6Br2O2. It is a benzoic acid derivative, featuring two bromine atoms at the 3 and 5 positions, and a methyl group at the 4 position on the benzene ring. 3,5-DIBROMO-4-METHYLBENZOIC ACID is known for its versatile applications in various industries due to its unique chemical structure and properties.

67973-32-4

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67973-32-4 Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIBROMO-4-METHYLBENZOIC ACID is used as an intermediate in the synthesis of pharmaceuticals for its potential antimicrobial and antifungal properties. It plays a crucial role in the development of new drugs targeting various infections and diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DIBROMO-4-METHYLBENZOIC ACID is utilized as an intermediate in the production of agrochemicals. Its properties contribute to the development of effective pesticides, herbicides, and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used in Dye Industry:
3,5-DIBROMO-4-METHYLBENZOIC ACID is employed as a building block in the synthesis of dyes, contributing to the creation of a wide range of colorants used in various applications, including textiles, plastics, and printing inks.
Used in Advanced Materials and Specialty Chemicals Production:
3,5-DIBROMO-4-METHYLBENZOIC ACID is also used as a key component in the production of advanced materials and specialty chemicals. Its unique structure and properties make it suitable for developing high-performance materials for various applications, such as coatings, adhesives, and composites.

Check Digit Verification of cas no

The CAS Registry Mumber 67973-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,7 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67973-32:
(7*6)+(6*7)+(5*9)+(4*7)+(3*3)+(2*3)+(1*2)=174
174 % 10 = 4
So 67973-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Br2O2/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3H,1H3,(H,11,12)

67973-32-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B25390)  3,5-Dibromo-4-methylbenzoic acid, 98+%   

  • 67973-32-4

  • 1g

  • 415.0CNY

  • Detail
  • Alfa Aesar

  • (B25390)  3,5-Dibromo-4-methylbenzoic acid, 98+%   

  • 67973-32-4

  • 5g

  • 986.0CNY

  • Detail

67973-32-4SDS

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 3,5-Dibromo-4-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-DIBROMO-4-METHYLBENZOIC ACID

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:67973-32-4 SDS

67973-32-4Relevant academic research and scientific papers

Pyrazolopyrimidines as dual Akt/p70S6K inhibitors

Rice, Kenneth D.,Kim, Moon H.,Bussenius, Joerg,Anand, Neel K.,Blazey, Charles M.,Bowles, Owen J.,Canne-Bannen, Lynne,Chan, Diva S.-M.,Chen, Baili,Co, Erick W.,Costanzo, Simona,Defina, Steven C.,Dubenko, Larisa,Engst, Stefan,Franzini, Maurizio,Huang, Ping,Jammalamadaka, Vasu,Khoury, Richard G.,Klein, Rhett R.,Laird, A.Douglas,Le, Donna T.,Mac, Morrison B.,Matthews, David J.,Markby, David,Miller, Nicole,Nuss, John M.,Parks, Jason J.,Tsang, Tsze H.,Tsuhako, Amy L.,Wang, Yong,Xu, Wei

supporting information; scheme or table, p. 2693 - 2697 (2012/05/20)

Activation of the PI3K/Akt/mTOR kinase pathway is frequently associated with human cancer. Selective inhibition of p70S6Kinase, which is the last kinase in the PI3K pathway, is not sufficient for strong tumor growth inhibition and can lead to activation of upstream proteins including Akt through relief of a negative feedback loop. Targeting multiple sites in the PI3K pathway might be beneficial for optimal activity. In this manuscript we report the design of dual Akt/p70S6K inhibitors and the evaluation of the lead compound 11b in vivo, which was eventually advanced into clinical development.

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