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4-Chloro-2-(trifluoromethyl)benzyl alcohol is a chemical compound characterized by the molecular formula C9H7ClF3O. It is a colorless to pale yellow liquid known for its strong antibacterial and antifungal properties. 4-CHLORO-2-(TRIFLUOROMETHYL)BENZYL ALCOHOL serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and is utilized as a reagent in organic synthesis and a building block for the production of other chemical compounds. Its versatility and bioactivity make it a valuable ingredient in various applications.

773872-13-2

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773872-13-2 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-2-(trifluoromethyl)benzyl alcohol is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs for treating bacterial and fungal infections. Its strong antibacterial and antifungal properties make it a promising candidate for medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Chloro-2-(trifluoromethyl)benzyl alcohol is employed as an intermediate in the production of agrochemicals, helping to develop effective solutions for controlling bacterial and fungal infections in crops and agricultural settings.
Used as a Reagent in Organic Synthesis:
4-Chloro-2-(trifluoromethyl)benzyl alcohol is utilized as a reagent in organic synthesis, facilitating the production of a wide range of chemical compounds. Its unique structure and properties make it a valuable component in various chemical reactions.
Used in Disinfectant Formulation:
Due to its strong antibacterial and antifungal properties, 4-Chloro-2-(trifluoromethyl)benzyl alcohol is used as an active ingredient in the formulation of disinfectants and antimicrobial products. It helps to ensure cleanliness and prevent the spread of infections in various settings, such as healthcare facilities, households, and public spaces.
Used in Chemical Compound Production:
4-Chloro-2-(trifluoromethyl)benzyl alcohol serves as a building block in the production of other chemical compounds, contributing to the creation of a diverse range of products with various applications across different industries. Its versatility and reactivity make it an essential component in the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 773872-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,8,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773872-13:
(8*7)+(7*7)+(6*3)+(5*8)+(4*7)+(3*2)+(2*1)+(1*3)=202
202 % 10 = 2
So 773872-13-2 is a valid CAS Registry Number.

773872-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-Chloro-2-(trifluoromethyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names JRD-1313

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:773872-13-2 SDS

773872-13-2Downstream Products

773872-13-2Relevant academic research and scientific papers

DEUTERIUM ATOM-SUBSTITUTED INDOLE FORMAMIDE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL APPLICATIONS THEREOF

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Paragraph 0101; 0108; 0110-0111, (2020/08/01)

A deuterium atom-substituted indole formamide derivative, a preparation method therefor, and medical applications thereof. Specifically, the present invention relates to a deuterium atom-substituted indole formamide derivative represented by general formula (I), a preparation method therefor, a pharmaceutical composition containing the derivative, and uses of the derivative serving as an ROR agonist and uses of the derivative in preventing and/or treating tumors or cancers, definitions of substituent groups in general formula (I) being same as definitions in the specification.

Hydrophilic group-substituted indole carboxamide derivative, preparation method thereof and application of hydrophilic group-substituted indole carboxamide derivative to medicine

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Paragraph 0230-0235, (2019/04/09)

The invention relates to a hydrophilic group-substituted indole carboxamide derivative, a preparation method thereof and application of the hydrophilic group-substituted indole carboxamide derivativeto medicine, particularly to a hydrophilic group-substituted indole carboxamide derivative shown as the formula (I), a preparation method thereof and a drug composition comprising the hydrophilic group-substituted indole carboxamide derivative. Besides, the invention also relates to application of the hydrophilic group-substituted indole carboxamide derivative as an ROR (retinoid-related orphan receptors) agonist as well as to preventing and/or treating tumor or cancer. The substituent groups in the formula (1) are identical in definition in those in specifications.

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