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(4-(4-(TrifluoroMethyl)phenoxy)phenyl)Methanol is a phenylmethanol chemical compound characterized by a phenyl ring with a trifluoromethyl group attached to one of the phenyl rings and a methanol group attached to the other phenyl ring. This unique structure and reactivity make it valuable for various applications in organic synthesis and pharmaceutical research.

933786-79-9

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933786-79-9 Usage

Uses

Used in Organic Synthesis:
(4-(4-(TrifluoroMethyl)phenoxy)phenyl)Methanol is used as a building block for the synthesis of complex organic molecules, taking advantage of its unique structure and reactivity.
Used in Pharmaceutical Research:
(4-(4-(TrifluoroMethyl)phenoxy)phenyl)Methanol is used as a starting material in the development of new drugs, particularly due to its trifluoromethyl group, which is valuable for medicinal chemistry and the development of bioactive molecules.
Used in Medicinal Chemistry:
(4-(4-(TrifluoroMethyl)phenoxy)phenyl)Methanol is used as a key intermediate in the synthesis of various bioactive molecules, contributing to the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 933786-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,7,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 933786-79:
(8*9)+(7*3)+(6*3)+(5*7)+(4*8)+(3*6)+(2*7)+(1*9)=219
219 % 10 = 9
So 933786-79-9 is a valid CAS Registry Number.

933786-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-(4-(Trifluoromethyl)phenoxy)phenyl)methanol

1.2 Other means of identification

Product number -
Other names [4-[4-(trifluoromethyl)phenoxy]phenyl]methanol

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:933786-79-9 SDS

933786-79-9Relevant academic research and scientific papers

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

2,6-DISUBSTITUTED PYRIDINES AS SOLUBLE GUANYLATE CYCLASE ACTIVATORS

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Page/Page column 64, (2009/07/17)

Disclosed are compounds of formula (I) wherein R1 and R2 are independently selected from hydrogen, halo, CF3, C1-4alkyl and allyl; Y represents (II), (III), (IV) or (V) wherein R3 represents CF3 or C1-4alkyl; and R3a represents CF3 or C1-4alkyl.

SOLUBLE GUANYLATE CYCLASE ACTIVATORS

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Page/Page column 20, (2009/09/05)

A compound having the structure useful for treatment or prevention of cardiovascular diseases, endothelial dysfunction, diastolic dysfunction, atherosclerosis, hypertension, angina pectoris, thromboses, restenoses, myocardial infarction, strokes, cardiac insufficiency, pulmonary hypertonia, erectile dysfunction, asthma bronchiale, chronic kidney insufficiency, diabetes, or cirrhosis of the liver in a human or animal patient.

4-OXY-N-[1 ,3,4]-THIADIAZOL-2-YL-BENZENE SULFONAMIDES, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS

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Page/Page column 65, (2008/06/13)

The invention relates to 4-oxy-N-[1 ,3,4]-thiadiazol-2-yl-benzene sulfonamides and to their physiologically acceptable salts and physiologically functional derivatives showing PPARalpha, PPARdelta and PPARgamma agonist activity. What is described are comp

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