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394-29-6

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394-29-6 Usage

Description

5-CHLORO-2-FLUOROBENZOYL CHLORIDE is an organic compound characterized by its chemical structure, which features a benzene ring with a chlorine atom at the 5th position and a fluorine atom at the 2nd position. Additionally, it has a benzoyl chloride functional group attached to the benzene ring. 5-CHLORO-2-FLUOROBENZOYL CHLORIDE is known for its colorless liquid state and is commonly utilized as a pharmaceutical intermediate due to its versatile chemical properties.

Uses

Used in Pharmaceutical Industry:
5-CHLORO-2-FLUOROBENZOYL CHLORIDE is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to be a key component in the development of new pharmaceutical compounds, contributing to the advancement of medical treatments.
Used in Chemical Synthesis:
As a versatile organic compound, 5-CHLORO-2-FLUOROBENZOYL CHLORIDE is also used in chemical synthesis for the production of other organic compounds. Its reactivity and functional groups make it a valuable building block for creating a wide range of chemical products, including those used in various industries such as agriculture, materials science, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 394-29-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 394-29:
(5*3)+(4*9)+(3*4)+(2*2)+(1*9)=76
76 % 10 = 6
So 394-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl2FO/c8-4-1-2-6(10)5(3-4)7(9)11/h1-3H

394-29-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
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  • Alfa Aesar

  • (B23273)  5-Chloro-2-fluorobenzoyl chloride, 97%   

  • 394-29-6

  • 1g

  • 312.0CNY

  • Detail
  • Alfa Aesar

  • (B23273)  5-Chloro-2-fluorobenzoyl chloride, 97%   

  • 394-29-6

  • 5g

  • 1127.0CNY

  • Detail
  • Aldrich

  • (535974)  5-Chloro-2-fluorobenzoylchloride  97%

  • 394-29-6

  • 535974-1ML

  • 911.43CNY

  • Detail

394-29-6Relevant articles and documents

Preparation method and application of tetrahydrobenzothiophene compound and pharmaceutical composition

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Paragraph 0187; 0190-0191; 0268; 0271-0272, (2021/10/16)

The invention belongs to the field of medicines, and particularly relates to a tetrahydrobenzothiophene compound as well as a pharmaceutical composition and a preparation method and application thereof. The tetrahydrobenzothiophene compound is a compound I as shown I. In-flight R1 And R2 The C1 -4 is a saturated/unsaturated hydrocarbon group. - OCH3 , OCH2 CH3 Phenyl, substituted phenyl, NO2 One - COR of - OH - F, Cl - Br. I - H R1 AND R2 Or different. R3 It is-F. - Cl, Br, I, OH, Amino, C1 -4 saturated/unsaturated hydrocarbon group, OCH3 , OCH2 CH3 , H, Wherein one of them is, n ≥ 5, n Being an integer. The compound effectively inhibits salmonella by inhibiting the synthesis of ATP-dependent transporter in the lipopolysaccharide synthesis pathway. Aeruginosa, escherichia coli and staphylococcus aureus.

COMPOUNDS THAT INHIBIT MCL-1 PROTEIN

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Page/Page column 106, (2017/09/15)

Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

Polymer electrolyte membranes based on poly(phenylene ether)s with sulfonic acid via long alkyl side chains

Zhang, Xuan,Sheng, Li,Hayakawa, Teruaki,Ueda, Mitsuru,Higashihara, Tomoya

, p. 11389 - 11396 (2013/09/23)

A series of poly(phenylene ether)s with sulfonic acid groups via long alkyl side chains, SPPEs, were successfully prepared as proton exchange membranes for fuel cells. The new monomer, bis[4-fluoro-3-(p-methoxylbenzoyl)]biphenyl (BFMBP), containing two pe

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