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197507-22-5

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197507-22-5 Usage

Uses

Methyl 2-fluoro-4-hydroxybenzoate can be used in the preparation of compounds, with the ability to inhibit cytosolic phospholipase A2α. It is also an intermediate in the synthesis of 3-(2-fluoro-4-hydroxyphenyl)-5-(trifluoromethyl) -4-isoxazolecarboxylic acid methyl ester (F591865).

Check Digit Verification of cas no

The CAS Registry Mumber 197507-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,5,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 197507-22:
(8*1)+(7*9)+(6*7)+(5*5)+(4*0)+(3*7)+(2*2)+(1*2)=165
165 % 10 = 5
So 197507-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO3/c1-12-8(11)6-3-2-5(10)4-7(6)9/h2-4,10H,1H3

197507-22-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H61675)  Methyl 2-fluoro-4-hydroxybenzoate, 98%   

  • 197507-22-5

  • 250mg

  • 338.0CNY

  • Detail
  • Alfa Aesar

  • (H61675)  Methyl 2-fluoro-4-hydroxybenzoate, 98%   

  • 197507-22-5

  • 1g

  • 1350.0CNY

  • Detail
  • Alfa Aesar

  • (H61675)  Methyl 2-fluoro-4-hydroxybenzoate, 98%   

  • 197507-22-5

  • 5g

  • 5487.0CNY

  • Detail

197507-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-fluoro-4-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names 2-fluoro-4-hydroxybenzoic acid methyl ester

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:197507-22-5 SDS

197507-22-5Relevant articles and documents

NOVEL COMPOUNDS FOR THE TREATMENT OF PARASITIC INFECTIONS

-

Page/Page column 66, (2019/08/14)

The present invention relates to novel compounds or pharmaceutically acceptable salts thereof, corresponding compositions, and methods and/or uses in therapy, for example in the treatment of parasitic infections such as malaria, in particular infection by

Synergistic Photo-Copper-Catalyzed Hydroxylation of (Hetero)aryl Halides with Molecular Oxygen

Zhang, Xin,Wu, Ge,Gao, Wenxia,Ding, Jinchang,Huang, Xiaobo,Liu, Miaochang,Wu, Huayue

supporting information, p. 708 - 711 (2018/02/09)

Photoredox-mediated copper-catalyzed hydroxylation of (hetero)aryl halides (including chlorides, bromides, and iodides) with O2 at room temperature has been developed. Preliminary mechanistic studies indicate no arylcopper intermediate and that aryl radicals are involved in this procedure. 18O-labeling experiments confirm the hydroxyl oxygen atom originated from molecular oxygen.

Synthesis and Structure-Activity Relationship Studies of Derivatives of the Dual Aromatase-Sulfatase Inhibitor 4-{[(4-Cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]methyl}phenyl sulfamate

Woo, L. W. Lawrence,Wood, Paul M.,Bubert, Christian,Thomas, Mark P.,Purohit, Atul,Potter, Barry V. L.

, p. 779 - 799 (2013/08/25)

4-{[(4-Cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]methyl}phenyl sulfamate and its ortho-halogenated (F, Cl, Br) derivatives are first-generation dual aromatase and sulfatase inhibitors (DASIs). Structure-activity relationship studies were performed on these

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