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4-CHLORO-6-FLUORO-2H-BENZOPYRAN-3-CARBOXALDEHYDE is a chemical compound with a molecular formula C15H9ClO3F. It is a benzopyran derivative that contains both chlorine and fluorine atoms. As a carboxaldehyde, it features an aldehyde group and a carboxylic acid group in its structure. This unique composition and reactivity make it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. The presence of chlorine and fluorine atoms in the molecule enhances its potential for developing new drugs and exploring its biological activities, making it significant for research and development in organic chemistry.

105799-69-7

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105799-69-7 Usage

Uses

Used in Pharmaceutical Industry:
4-CHLORO-6-FLUORO-2H-BENZOPYRAN-3-CARBOXALDEHYDE is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity. The presence of chlorine and fluorine atoms in the molecule allows for the development of new drugs with potential biological activities.
Used in Agrochemical Industry:
4-CHLORO-6-FLUORO-2H-BENZOPYRAN-3-CARBOXALDEHYDE is used as a building block in the synthesis of agrochemicals, contributing to the development of new compounds with potential applications in agriculture.
Used in Medicinal Chemistry Research:
4-CHLORO-6-FLUORO-2H-BENZOPYRAN-3-CARBOXALDEHYDE is used as a research compound in medicinal chemistry for exploring its potential biological activities and developing new drugs based on its unique structure.
Used in Organic Chemistry Research and Development:
4-CHLORO-6-FLUORO-2H-BENZOPYRAN-3-CARBOXALDEHYDE is used as a research compound in the field of organic chemistry for further exploration of its reactivity and potential applications in the synthesis of various compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 105799-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,7,9 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105799-69:
(8*1)+(7*0)+(6*5)+(5*7)+(4*9)+(3*9)+(2*6)+(1*9)=157
157 % 10 = 7
So 105799-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClFO2/c11-10-6(4-13)5-14-9-2-1-7(12)3-8(9)10/h1-4H,5H2

105799-69-7 Well-known Company Product Price

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  • Aldrich

  • (543721)  4-Chloro-6-fluoro-2H-benzopyran-3-carboxaldehyde  97%

  • 105799-69-7

  • 543721-1G

  • 1,123.20CNY

  • Detail

105799-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-fluoro-2H-chromene-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Chloro-6-Fluoro-2H-1-Benzopyran-3-Carboxaldehyde

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:105799-69-7 SDS

105799-69-7Relevant articles and documents

4H-Thieno[3,2-c]chromene based inhibitors of Notum Pectinacetylesterase

Han, Qiang,Pabba, Praveen K.,Barbosa, Joseph,Mabon, Ross,Healy, Jason P.,Gardyan, Michael W.,Terranova, Kristen M.,Brommage, Robert,Thompson, Andrea Y.,Schmidt, James M.,Wilson, Alan G.E.,Xu, Xiaolian,Tarver, James E.,Carson, Kenneth G.

, p. 1184 - 1187 (2016)

A group of small molecule thienochromenes inhibitors of Notum Pectinacetylesterase are described. We developed SAR on three series based on carbon, oxygen and sulfur replacement of the 5-position. In each series, highly potent Notum Pectinacetylesterase inhibitors were identified.

Synthesis of Pyrazolo[1,5-a]pyrimido[4,3-d]benzopyrans and 2-Pyrazolo [1,5-a]pyrimidinylphenols from the reaction of 5(3)-amino pyrazoles

Jagath Reddy,Latha,Pallavi,Srinivasa Rao,Khalilullah

, p. 453 - 456 (2007/10/03)

A number of Pyrazolo[1,5-a]pyrimido[4,3-d]benzopyrans(4a-m) and 2-(Pyrazolo[1,5-a]pyrimidinyl)phenols (7a-k) have been prepared from the reaction of 5(3)-aminopyrazoles 3.

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