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6-CHLORO-2,3-DIFLUOROBENZALDEHYDE is a chemical compound characterized by the molecular formula C7H3ClF2O. It is a pale yellow liquid with a strong odor, known for its aldehyde group, which is instrumental in the synthesis of various organic compounds. 6-CHLORO-2,3-DIFLUOROBENZALDEHYDE is primarily recognized for its role as an intermediate in the production of pharmaceuticals and agrochemicals, and it is also utilized as a building block in the preparation of fluorinated benzaldehyde derivatives with diverse industrial and medicinal applications. Its significance in the field of organic chemistry is further underscored by its use as a starting material in the synthesis of biologically active compounds.

797791-33-4

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797791-33-4 Usage

Uses

Used in Pharmaceutical Industry:
6-CHLORO-2,3-DIFLUOROBENZALDEHYDE is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a wide range of medicinal compounds with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 6-CHLORO-2,3-DIFLUOROBENZALDEHYDE serves as a key intermediate in the production of agrochemicals, such as pesticides and herbicides. Its role in these applications is crucial for enhancing crop protection and improving agricultural productivity.
Used in Organic Chemistry Research:
6-CHLORO-2,3-DIFLUOROBENZALDEHYDE is utilized as a building block in the preparation of fluorinated benzaldehyde derivatives, which are valuable in various industrial applications. Its presence in these derivatives expands the scope of organic chemistry, enabling the exploration of new chemical reactions and the synthesis of novel compounds with unique properties.
Used in Synthesis of Biologically Active Compounds:
6-CHLORO-2,3-DIFLUOROBENZALDEHYDE is employed as a starting material in the synthesis of biologically active compounds, which have potential applications in medicine, biotechnology, and other related fields. Its versatility in this context highlights its importance in the discovery and development of new bioactive substances with therapeutic or other beneficial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 797791-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,7,7,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 797791-33:
(8*7)+(7*9)+(6*7)+(5*7)+(4*9)+(3*1)+(2*3)+(1*3)=244
244 % 10 = 4
So 797791-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClF2O/c8-5-1-2-6(9)7(10)4(5)3-11/h1-3H

797791-33-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H34287)  6-Chloro-2,3-difluorobenzaldehyde, 97%   

  • 797791-33-4

  • 1g

  • 664.0CNY

  • Detail
  • Alfa Aesar

  • (H34287)  6-Chloro-2,3-difluorobenzaldehyde, 97%   

  • 797791-33-4

  • 5g

  • 2646.0CNY

  • Detail

797791-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLORO-2,3-DIFLUOROBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names Benzaldehyde,6-chloro-2,3-difluoro

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:797791-33-4 SDS

797791-33-4Upstream product

797791-33-4Relevant academic research and scientific papers

Ortho substituted benzaldehydes, preparation thereof and use thereof

-

, (2008/06/13)

Compounds of the formula (I) in which X1=H or F, X2=H or F, and Y=Cl, Br or I, are prepared by reacting, in a solvent or solvent mixture at a temperature below ?60° C., a halobenzene of the formula (II) with an organic lithium compou

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