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Methyl 5-bromo-2-(trifluoromethoxy)benzoate is a synthetic, organic chemical compound belonging to the benzoate esters group. It features a benzoate functional group along with bromine, fluorine, and methoxy groups, which impart unique chemical properties to the molecule. These properties, such as polarity, solubility, and reactivity, may influence its potential use in various chemical reactions, synthesis procedures, or as a reagent. However, specific applications, hazard classifications, or detailed physical and chemical properties are not widely documented, indicating that it is likely a specialized, niche chemical used in specific research or industrial applications.

773874-13-8

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773874-13-8 Usage

Uses

Used in Chemical Synthesis:
Methyl 5-bromo-2-(trifluoromethoxy)benzoate is used as a reagent or intermediate in chemical synthesis processes due to its unique chemical properties, which may facilitate specific reactions or contribute to the formation of desired products.
Used in Research Applications:
As a specialized, niche chemical, methyl 5-bromo-2-(trifluoromethoxy)benzoate is used in research settings to explore its potential applications and properties. This may include studying its reactivity, solubility, or interactions with other compounds in various chemical systems.
Used in Industrial Applications:
Although specific uses are not widely documented, methyl 5-bromo-2-(trifluoromethoxy)benzoate may be employed in certain industrial applications where its unique attributes can be leveraged for specific purposes, such as in the development of new materials or processes.

Check Digit Verification of cas no

The CAS Registry Mumber 773874-13-8 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 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773874-13:
(8*7)+(7*7)+(6*3)+(5*8)+(4*7)+(3*4)+(2*1)+(1*3)=208
208 % 10 = 8
So 773874-13-8 is a valid CAS Registry Number.

773874-13-8SDS

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 Methyl 5-bromo-2-(trifluoromethoxy)benzoate

1.2 Other means of identification

Product number -
Other names 5-bromo-2-trifluoromethoxy-benzoic acid methyl ester

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:773874-13-8 SDS

773874-13-8Relevant academic research and scientific papers

COMPOUNDS AND THEIR METHODS OF USE

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Page/Page column 212-213, (2018/06/12)

The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including Dravet syndrome or epilepsy are also provided herein.

Alpha-alkyl substituted N-acyltryptophanols

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Page/Page column 44, (2009/03/07)

The present invention relates to α-alkyl substituted N-acyltryptophanols of the formula I in which R1, R2, R3, R4, R5, R6, Q, X and W have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example for fertility control in men or in women, or for the prevention and/or treatment of osteoporosis.

Cyanomethyl substituted N-Acyl Tryptamines

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Page/Page column 36, (2009/03/07)

The present invention relates to cyanomethyl substituted N-acyl tryptamines of the formula I in which R1, R2, R3, R4, R5, Q, X and W have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and

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