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3-Chloro-4,5-difluoronitrobenzene is a chemical compound with the molecular formula C6H3ClF2NO2. It is a nitrobenzene derivative characterized by the presence of a chlorine atom in the ortho position and two fluorine atoms in the para positions of the benzene ring. 3-Chloro-4,5-difluoronitrobenzene is known for its versatile applications in various industries, primarily as an intermediate in the synthesis of pharmaceuticals, agrochemicals, dyes, and pigments. However, due to its toxic and potentially harmful properties, it is classified as a hazardous chemical and requires careful handling.

53780-44-2

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53780-44-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4,5-difluoronitrobenzene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved therapeutic properties and reduced side effects. 3-Chloro-4,5-difluoronitrobenzene's reactivity and functional groups make it an ideal candidate for further chemical modifications, enabling the creation of novel pharmaceutical agents.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chloro-4,5-difluoronitrobenzene serves as an essential intermediate for the production of various agrochemicals, including pesticides and herbicides. Its incorporation into these compounds enhances their effectiveness in controlling pests and weeds, thereby contributing to increased crop yields and improved agricultural productivity.
Used in Dye and Pigment Production:
3-Chloro-4,5-difluoronitrobenzene is utilized in the manufacturing process of dyes and pigments due to its ability to impart vibrant colors and excellent stability. Its presence in these products ensures their resistance to fading, making them suitable for various applications, such as textiles, plastics, and coatings.
Used in Chemical Research:
3-Chloro-4,5-difluoronitrobenzene is also employed as a valuable research tool in the field of organic chemistry. Its unique structure and reactivity make it an ideal candidate for studying various chemical reactions and mechanisms. Researchers use 3-Chloro-4,5-difluoronitrobenzene to explore new synthetic routes, develop innovative methodologies, and gain insights into the fundamental principles of chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 53780-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,8 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53780-44:
(7*5)+(6*3)+(5*7)+(4*8)+(3*0)+(2*4)+(1*4)=132
132 % 10 = 2
So 53780-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H2ClF2NO2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H

53780-44-2SDS

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 3-Chloro-4,5-difluoronitrobenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-2,3-difluoro-5-nitrobenzene

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:53780-44-2 SDS

53780-44-2Upstream product

53780-44-2Downstream Products

53780-44-2Relevant academic research and scientific papers

Synthesis of fluorinated halonitrobenzenes and halonitrophenols using tetrafluoroethylene and buta-1,3-dienes as starting building blocks

Lipkind, M. B.,Nefedov, O. M.,Volchkov, N. V.

, p. 2156 - 2163 (2022/01/22)

The gas-phase copyrolysis of tetrafluoroethylene with buta-1,3-diene in a flow reactor at 495–505 °C produces 3,3,4,4-tetrafluorocyclohex-1-ene, which selectively converted to 1,2-difluorobenzene or 1-chloro-2,3-difluorobenzene. The latter can be converted to 2-chloro-3,4-difluoronitrobenzene, 2,3,4-trifluoronitrobenzene, 2,3-difluoro-6-nitrophenol, or 2-chloro-3-fluoro-4-nitrophenol via nitration, fluorodechlorination, and hydrolysis reactions.

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