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2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide is a chemical compound with the formula C14H9ClF3NO. It is a benzamide derivative featuring a chlorine atom and a trifluoromethyl group attached to the aromatic ring. 2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide is known for its unique chemical properties, which make it a versatile building block in various chemical processes.

3873-78-7

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3873-78-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide is used as an intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, potentially contributing to the creation of medications with novel therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, 2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide is utilized as an intermediate for the production of various agrochemicals. Its properties make it suitable for the development of compounds that can be used in agriculture to protect crops and enhance yields.
Used in Organic Compounds Production:
2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide is also used as an intermediate in the production of other organic compounds. Its versatility in chemical reactions allows it to be a valuable precursor for synthesizing a wide range of organic molecules for different applications.
Used in Medicinal Chemistry:
Due to its unique chemical properties, 2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide may have applications in medicinal chemistry. Researchers can explore its potential use in the design and synthesis of new pharmaceutical agents, targeting specific diseases and conditions.
Used in Agriculture:
In the field of agriculture, 2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide can be employed in the development of agrochemicals that help improve crop protection and increase productivity. Its role in this industry is crucial for ensuring food security and sustainable agricultural practices.
Used in Materials Science:
2-chloro-N-[2-(trifluoromethyl)phenyl]benzamide's unique properties also make it a potential candidate for applications in materials science. Researchers can investigate its use in the development of new materials with specific properties, such as improved stability, reactivity, or other characteristics that can be beneficial in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3873-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3873-78:
(6*3)+(5*8)+(4*7)+(3*3)+(2*7)+(1*8)=117
117 % 10 = 7
So 3873-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H9ClF3NO/c15-11-7-3-1-5-9(11)13(20)19-12-8-4-2-6-10(12)14(16,17)18/h1-8H,(H,19,20)

3873-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-benzoic acid-(2-trifluoromethyl-anilide)

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-chloro,2-chloroethyl 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:3873-78-7 SDS

3873-78-7Downstream Products

3873-78-7Relevant academic research and scientific papers

Visible-Light Mediated ortho-Trifluoromethylation of Aniline Derivatives

Tian, Chao,Wang, Qiyue,Wang, Xueqi,An, Guanghui,Li, Guangming

, p. 14241 - 14247 (2019/10/16)

A general visible-light mediated ortho-C-H trifluoromethylation of aniline derivatives by using a low-cost and stable Langlois reagent (CF3SO2Na) as the "CF3" source has been developed. In contrast to previous reports, this strategy allowed access to elusive trifluoromethyl lactams. Furthermore, mechanism experiments revealed that a copper/photoredox dual catalytic mechanism enabled general trifluoromethylation of aniline derivatives.

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