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167091-96-5

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167091-96-5 Usage

Description

[4-(4-fluorophenoxy)phenyl]methanol is a chemical compound that belongs to the class of phenylmethanols. It is characterized by a phenyl ring substituted with a 4-fluorophenoxy group and a hydroxyl group attached to the methylene carbon. [4-(4-fluorophenoxy)phenyl]methanol is known for its unique properties and potential biological activity, particularly due to the presence of a fluorine atom on the phenyl ring.

Uses

Used in Pharmaceutical Industry:
[4-(4-fluorophenoxy)phenyl]methanol is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and the presence of a fluorine atom make it an interesting target for medicinal chemistry and drug discovery research.
Used in Agrochemical Industry:
In the agrochemical industry, [4-(4-fluorophenoxy)phenyl]methanol is utilized as a starting material for the development of new agrochemicals, contributing to the creation of innovative products for agricultural applications.
Used in Organic Chemistry:
[4-(4-fluorophenoxy)phenyl]methanol serves as a valuable building block in the field of organic chemistry, enabling the synthesis of a wide range of fine chemicals with diverse applications.
Used in Material Science:
With its unique properties, [4-(4-fluorophenoxy)phenyl]methanol has potential applications in the development of new materials, where its fluorine-containing structure may offer advantages in terms of reactivity, stability, or other material properties.
Used as a Reagent in Organic Transformations:
In addition to its applications in various industries, [4-(4-fluorophenoxy)phenyl]methanol can also be employed as a reagent in organic transformations, facilitating specific chemical reactions and contributing to the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 167091-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,0,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 167091-96:
(8*1)+(7*6)+(6*7)+(5*0)+(4*9)+(3*1)+(2*9)+(1*6)=155
155 % 10 = 5
So 167091-96-5 is a valid CAS Registry Number.

167091-96-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H33388)  4-(4-Fluorophenoxy)benzyl alcohol, 97%   

  • 167091-96-5

  • 1g

  • 1037.0CNY

  • Detail
  • Alfa Aesar

  • (H33388)  4-(4-Fluorophenoxy)benzyl alcohol, 97%   

  • 167091-96-5

  • 5g

  • 3449.0CNY

  • Detail

167091-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-Fluorophenoxy)phenyl]methanol

1.2 Other means of identification

Product number -
Other names 4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)-2,2-diphenylbutanenitrile

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:167091-96-5 SDS

167091-96-5Relevant articles and documents

Synthesis and Structure-Activity Relationships for Extended Side Chain Analogues of the Antitubercular Drug (6 S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5 H -imidazo[2,1- b ][1,3]oxazine (PA-824)

Palmer, Brian D.,Sutherland, Hamish S.,Blaser, Adrian,Kmentova, Iveta,Franzblau, Scott G.,Wan, Baojie,Wang, Yuehong,Ma, Zhenkun,Denny, William A.,Thompson, Andrew M.

, p. 3036 - 3059 (2015/04/27)

Novel extended side chain nitroimidazooxazine analogues featuring diverse linker groups between two aryl rings were studied as a potential strategy to improve solubility and oral activity against chronic infection by Mycobacterium tuberculosis. Both lipop

THIAZOLE COMPOUNDS AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

-

Page/Page column 54, (2010/04/03)

Disclosed are compounds of formula (I) wherein R1 and R2 are independently selected from hydrogen, halo, C1-4alkyl, C1-4alkoxy, CF3 and OCF3; -Y- represents formula (IA) R3 represents hydrogen, fluoro, chloro or C1-4alkyl; R4a and R4b each independently represent hydrogen, C1-4alkyl, C1-4alkoxy, CF3 or halo; and R5 represents a group Z-X; wherein Z is absent or represents (CH2)2 or O; and X represents formula (IB) wherein: J and L both represent CH, or one of J and L represents CH and the other represents N; when both J and L represent CH, R6 represents hydrogen, halo, CF3, C1-4alkyl or C1-4alkoxy in a meta or ortho position relative to the R7 substituent and R7 represents hydrogen, halo, CF3, OCF3, C1-4alkyl, C1-4alkoxy, CH2OH, CN, CONR8R9 or CO2H; or when one of J or L represents N, R6 represents hydrogen or halo in a meta or ortho position relative to the R7 substituent and R7 represents hydrogen, halo, CF3, C1-4alkyl, C1-4alkoxy, CH2OH, CN, CONR8R9 or CO2H; and R8 and R9 are independently selected from hydrogen and C1-4alkyl; or salts thereof which activate soluble guanylate cyclase (sGC), pharmaceutical compositions containing them, their use in medicine, and processes for their preparation.

PYRAZOLES AS HUMAN NON-PANCREATIC SECRETORY PHOSPHOLIPASE A2 INHIBITORS

-

, (2008/06/13)

A class of novel pyrazoles is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock

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