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81107-97-3

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81107-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81107-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,0 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81107-97:
(7*8)+(6*1)+(5*1)+(4*0)+(3*7)+(2*9)+(1*7)=113
113 % 10 = 3
So 81107-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrF3O/c8-5-3-4(7(9,10)11)1-2-6(5)12/h1-3,12H

81107-97-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H61836)  2-Bromo-4-(trifluoromethyl)phenol, 98%   

  • 81107-97-3

  • 1g

  • 305.0CNY

  • Detail
  • Alfa Aesar

  • (H61836)  2-Bromo-4-(trifluoromethyl)phenol, 98%   

  • 81107-97-3

  • 5g

  • 1221.0CNY

  • Detail

81107-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4-(Trifluoromethyl)Phenol

1.2 Other means of identification

Product number -
Other names 2-BROMO-4-(TRIFLUOROMETHYL)PHENOL

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:81107-97-3 SDS

81107-97-3Relevant articles and documents

Macrocyclic Modulators of the Ghrelin Receptor

-

Paragraph 0465, (2018/05/03)

The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.

Direct Conversion of Haloarenes to Phenols under Mild, Transition-Metal-Free Conditions

Fier, Patrick S.,Maloney, Kevin M.

supporting information, p. 2244 - 2247 (2016/06/01)

A high-yielding and practical method for the synthesis of phenols from electron-deficient haloarenes and heteroarenes has been developed. The products are formed from acetohydroxamic acid as the hydroxide source via a novel SNAr reaction/Lossen rearrangement sequence. Notably, these reactions employ inexpensive and air-stable reagents, require no special handling, occur under mildly basic conditions, and form products in high yields in the presence of electrophilic and protic functionality. The utility of this methodology is demonstrated by the high-yielding hydroxylation of two base-sensitive complex substrates.

2-PHENYL PHENOXYACETIC ACIDS USEFUL FOR TREATING INFLAMMATORY DISORDERS

-

Page/Page column 30-31, (2009/09/04)

The present invention provides novel phenoxyacetic acids useful for the prevention and treatment of inflammatory disorders, including those affecting the respiratory system and skin. The compounds are of the general formula (I):

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