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2-Bromo-4-(trifluoromethoxy)phenol, also known as trifluoromethoxyphenyl bromide, is a chemical compound with the formula C7H4BrF3O2. It is a white to light brown crystalline solid that is commonly used in the synthesis of pharmaceuticals and agrochemicals. This versatile chemical serves as a building block in organic synthesis, particularly in the production of drugs and herbicides, and is known for its antimicrobial and antifungal properties, making it useful in the development of new pharmaceutical products. It is also used as an intermediate in the manufacture of specialty chemicals and other organic compounds.

200956-13-4

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200956-13-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-4-(trifluoromethoxy)phenol is used as a building block in organic synthesis for the development of new pharmaceutical products. Its antimicrobial and antifungal properties contribute to the creation of drugs that target various infections and diseases.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Bromo-4-(trifluoromethoxy)phenol is used as a key component in the synthesis of herbicides. Its incorporation into these products helps in the effective control of unwanted plant growth, thereby enhancing crop productivity.
Used in Organic Synthesis:
2-Bromo-4-(trifluoromethoxy)phenol is utilized as an intermediate in the manufacture of specialty chemicals and other organic compounds. Its unique structure and properties make it a valuable component in the synthesis of a wide range of chemical products.
Overall, 2-Bromo-4-(trifluoromethoxy)phenol is a versatile and valuable chemical compound with applications spanning across various industries, particularly in the development and production of pharmaceuticals, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 200956-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,9,5 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 200956-13:
(8*2)+(7*0)+(6*0)+(5*9)+(4*5)+(3*6)+(2*1)+(1*3)=104
104 % 10 = 4
So 200956-13-4 is a valid CAS Registry Number.

200956-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-4-(trifluoromethoxy)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2-bromo-4-(trifluoromethoxy)

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:200956-13-4 SDS

200956-13-4Relevant articles and documents

Use of NK-1 receptor antagonists for treating major depressive disorders

-

, (2008/06/13)

The present invention provides methods for the treatment of major depressive disorders comprising oral administration of an orally active, long acting, CNS-penetrant NK-1 receptor antagonist and pharmaceutical compositions comprising such a NK-1 receptor

2-aryl indole derivative as antagonists of tachykinins

-

Page/Page column 26, (2008/06/13)

The present invention relates to compounds of the formula (I): wherein R1a, R1b, R2, R3, R4, R5, X and n are defined herein. The compounds are of particular use in the treatment or prevention of depression, anxiety, pain, inflammation, migraine, emesis and postherpetic neuralgia.

Stereocontrolled syntheses of epimeric 3-aryl-6-phenyl-1-oxa-7-azaspiro[4.5]decane NK-1 receptor antagonist precursors

Kulagowski, Janusz J.,Curtis, Neil R.,Swain, Christopher J.,Williams, Brian J.

, p. 667 - 670 (2007/10/03)

Equation presented Complementary stereoselective syntheses of individual C3 epimers of the NK-1 receptor antagonist precursor 1 have been developed. Both diastereomers were derived from the common intermediate 3; introduction of the 3S stereocenter in 1a

Use of NK-1 receptor antagonists for treating stress disorders

-

, (2008/06/13)

The present invention provides the use of an orally active, long acting, CNS-penetrant NK-1 receptor antagonist for the manufacture of a medicament adapted for oral administration for the treatment or prevention of stress disorders without concomitant the

Phenyl spiroethercycloalkyl tachykinin receptor antagonists

-

, (2008/06/13)

The present invention is directed to certain novel compounds represented by structural formula I: STR1 or a pharmaceutically acceptable salt thereof, wherein R 3, R 6, R 7, R 8, R 11, R 12, R 13, m, n and the dashed lines are defined herein. The invention is also concerned with pharmaceutical formulations comprising these novel compounds as active ingredients and the use of the novel compounds and their formulations in the treatment of certain disorders. The compounds of this invention are tachykinin receptor antagonists and are useful in the treatment of inflammatory diseases, pain or migraine, asthma and emesis.

USE OF NK-1 RECEPTOR ANTAGONISTS FOR TREATING BIPOLAR DISORDERS

-

, (2008/06/13)

The present invention provides methods for the treatment or prevention of bipolar disorder without concomitant therapy with other antidepressant or anti-anxiety agents which comprises oral administration of an orally active, long acting, CNS-penetrant NK-

1,3-benzoxazine derivatives, their production and use

-

, (2008/06/13)

A new compound of the formula: STR1 wherein STR2 is an optionally substituted benzene ring; R1 is a carbocyclic or heterocyclic group which is linked to the 4-position of the 1,3-benzoxazine ring through a carbon-carbon bond, a hydrocarbon resi

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