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4-BROMO-2-METHYLTHIOBENZAMIDE is a chemical compound characterized by the molecular formula C8H8BrNO2S. It is a white to off-white solid that serves as a crucial intermediate in the synthesis of various pharmaceuticals and organic compounds. This versatile compound is also utilized as a building block in the production of agrochemicals and specialty chemicals, making it valuable across multiple industries such as agriculture, pharmaceuticals, and materials science. Due to its chemical nature, it is essential to follow proper safety measures during its handling and storage to protect both workers and the environment.

397845-03-3

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397845-03-3 Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-2-METHYLTHIOBENZAMIDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and therapeutic agents. Its unique chemical structure allows it to be a part of complex molecular frameworks that can target specific biological pathways or receptors, potentially leading to the creation of more effective treatments for various diseases and conditions.
Used in Agrochemical Production:
In the agrochemical industry, 4-BROMO-2-METHYLTHIOBENZAMIDE is employed as a building block for the development of new pesticides, herbicides, and other crop protection agents. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases, thereby contributing to increased agricultural productivity and food security.
Used in Materials Science:
4-BROMO-2-METHYLTHIOBENZAMIDE is utilized in materials science for its potential to be integrated into the development of advanced materials with specific properties. Its unique chemical structure can be leveraged to create materials with improved characteristics such as enhanced stability, reactivity, or selectivity, which can be applied in various high-tech applications.
Used in Organic Compounds Synthesis:
4-BROMO-2-METHYLTHIOBENZAMIDE is used as a versatile building block in the synthesis of a wide range of organic compounds. Its reactivity and structural features make it a valuable component in the creation of complex organic molecules for various applications, including the development of new chemical processes, the production of specialty chemicals, and the synthesis of novel materials with unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 397845-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,7,8,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 397845-03:
(8*3)+(7*9)+(6*7)+(5*8)+(4*4)+(3*5)+(2*0)+(1*3)=203
203 % 10 = 3
So 397845-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNS/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4H,1H3,(H2,10,11)

397845-03-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H55421)  4-Bromo-2-methylthiobenzamide, 96%   

  • 397845-03-3

  • 1g

  • 246.0CNY

  • Detail
  • Alfa Aesar

  • (H55421)  4-Bromo-2-methylthiobenzamide, 96%   

  • 397845-03-3

  • 5g

  • 969.0CNY

  • Detail
  • Aldrich

  • (684740)  4-Bromo-2-methylthiobenzamide  96%

  • 397845-03-3

  • 684740-1G

  • 390.78CNY

  • Detail

397845-03-3Relevant articles and documents

Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets

Mayhoub, Abdelrahman S.,Marler, Laura,Kondratyuk, Tamara P.,Park, Eun-Jung,Pezzuto, John M.,Cushman, Mark

experimental part, p. 510 - 520 (2012/03/10)

Chemoprevention is an approach to decrease cancer morbidity and mortality through inhibition of carcinogenesis and prevention of disease progression. Although the trans stilbene derivative resveratrol has chemopreventive properties, its action is compromised by weak non-specific effects on many biological targets. Replacement of the stilbene ethylenic bridge of resveratrol with a 1,2,4-thiadiazole heterocycle and modification of the substituents on the two aromatic rings afforded potential chemopreventive agents with enhanced potencies and selectivities when evaluated as inhibitors of aromatase and NF-κB and inducers of quinone reductase 1 (QR1).

Synthesis and biological evaluation of a 5-6-5 imidazole-phenyl-thiazole based α-helix mimetic

Cummings, Christopher G.,Ross, Nathan T.,Katt, William P.,Hamilton, Andrew D.

supporting information; experimental part, p. 25 - 28 (2009/06/28)

The development of small molecules that disrupt protein-protein interactions is a key goal in addressing a number of disease states. The α-helix is commonly found at protein interaction interfaces and has been the focus of substantial small molecule mimet

NOVEL HERBICIDES

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Page/Page column 78-79, (2009/04/25)

Compounds of formula (I) wherein the substituents are as defined in claim 1, are suitable for use as herbicides.

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