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115029-22-6

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115029-22-6 Usage

Chemical Properties

White to beige crystalline powder

Uses

2-Fluoro-3-(trifluoromethyl)benzoic acid may be used in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 115029-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115029-22:
(8*1)+(7*1)+(6*5)+(5*0)+(4*2)+(3*9)+(2*2)+(1*2)=86
86 % 10 = 6
So 115029-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F4O2/c9-6-4(7(13)14)2-1-3-5(6)8(10,11)12/h1-3H,(H,13,14)/p-1

115029-22-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (B20280)  2-Fluoro-3-(trifluoromethyl)benzoic acid, 98%   

  • 115029-22-6

  • 1g

  • 364.0CNY

  • Detail
  • Alfa Aesar

  • (B20280)  2-Fluoro-3-(trifluoromethyl)benzoic acid, 98%   

  • 115029-22-6

  • 5g

  • 1199.0CNY

  • Detail
  • Alfa Aesar

  • (B20280)  2-Fluoro-3-(trifluoromethyl)benzoic acid, 98%   

  • 115029-22-6

  • 25g

  • 5326.0CNY

  • Detail

115029-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-FLUORO-3-(TRIFLUOROMETHYL)BENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Fluoro-3-trifluoromethyl-benzoic 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:115029-22-6 SDS

115029-22-6Relevant articles and documents

Discovery of Orally Bioavailable Ligand Efficient Quinazolindiones as Potent and Selective Tankyrases Inhibitors

Qin, Donghui,Lin, Xiaojuan,Liu, Zhi,Chen, Yan,Zhang, Zhiliu,Wu, Chengde,Liu, Linlin,Pan, Yan,Laquerre, Sylvie,Emery, John,Fergusson, Jeff,Roland, Kimberly,Keenan, Rick,Oliff, Allen,Kumar, Sanjay,Cheung, Mui,Su, Dai-Shi

, p. 1005 - 1010 (2021)

We report herein the discovery of quinazolindiones as potent and selective tankyrase inhibitors. Elucidation of the structure-activity relationship of the lead compound 1g led to truncated analogues that have good potency in cells, pharmacokinetic (PK) properties, and excellent selectivity. Compound 21 exhibited excellent potencies in cells and proliferation studies, good selectivity, in vitro activities, and an excellent PK profile. Compound 21 also inhibited H292 xenograft tumor growth in nude mice. The synthesis, biological, pharmacokinetic, in vivo efficacy studies, and safety profiles of compounds are presented.

P2X7 MODULATORS

-

Paragraph 0284; 0286, (2014/09/29)

The present invention is directed to compounds of Formulas (I, IIa and IIb): The invention also relates to pharmaceutical compositions comprising compounds of Formulas (I, IIa and IIb). Methods of making and using the compounds of Formulas (I, IIa and IIb) are also within the scope of the invention.

INHIBITORS OF STEAROYL-COA DESATURASE

-

, (2009/06/27)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.

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