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108940-98-3

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  • (2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydro-1-benzofuran-2-carboxylic acid

    Cas No: 108940-98-3

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108940-98-3 Usage

Description

(2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid is a benzofuran derivative with a molecular formula of C12H10Cl2O5S. It features two chlorine atoms and a dimethylsulfamoyl group, which contribute to its unique chemical properties. This chemical compound is currently under investigation for its potential biological activities and applications in pharmaceutical research.

Uses

Used in Pharmaceutical Research:
(2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid is used as a chemical compound in pharmaceutical research for its potential biological activities. The exact functions and applications of this compound are still under investigation, which may lead to the development of new drugs or therapies in the future.
Used in Chemical Synthesis:
As a benzofuran derivative with specific functional groups, (2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid can be used as a building block or intermediate in the synthesis of more complex organic compounds. Its unique structure may enable the creation of novel molecules with specific properties for various applications.
Used in Medicinal Chemistry:
The presence of chlorine atoms and the dimethylsulfamoyl group in (2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid may provide opportunities for medicinal chemists to explore its interactions with biological targets. This could lead to the discovery of new lead compounds or optimization of existing drug candidates for improved efficacy and selectivity.
Note: Since the exact functions and applications of (2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid are still under investigation, the uses listed above are speculative and based on the general properties of similar chemical compounds. Further research is required to confirm its potential applications and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 108940-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,4 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 108940-98:
(8*1)+(7*0)+(6*8)+(5*9)+(4*4)+(3*0)+(2*9)+(1*8)=143
143 % 10 = 3
So 108940-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11Cl2NO5S/c1-14(2)20(17,18)7-4-5-3-6(11(15)16)19-10(5)9(13)8(7)12/h4,6H,3H2,1-2H3,(H,15,16)/t6-/m1/s1

108940-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-6,7-dichloro-5-(dimethylsulfamoyl)-2,3-dihydrobenzofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:108940-98-3 SDS

108940-98-3Downstream Products

108940-98-3Relevant articles and documents

Optical Resolution and Chiral Synthesis of Methyl 6,7-Dichloro-2,3-dihydrobenzofuran-2-carboxylate

Yodo, Mitsuaki,Matsushita, Yoshihiro,Ohsugi, Eiichi,Harada, Hiroshi

, p. 902 - 913 (2007/10/02)

Optical isomers of methyl 6,7-dichloro-2,3-dibenzofuran-2-carboxylate (2) were prepared by means of both optical resolution and chiral synthesis.The resolution of the carboxylic acid 3 was achieved in a practical and efficient way via the l- and d-menthyl esters, which were directly converted to enantiomers of 2.Chiral synthesis of 2 was attained with high optical yield via acid-catalyzed cyclization of the β-hydroxysulfide 10 derived from optically active glycidyl phenyl sulfide 13.The optical resolution method was considered to be better for large-scale preparation from the economical and operational viewpoints.Keywords - methyl 6,7-dichloro-2,3-dibenzofuran-2-carboxylate; optical resolution; (R)-4-phenyl-2-oxazolidone; menthol; chiral synthesis; glycidyl phenyl sulfide; β-hydroxysulfide; episulfonium ion; S-8666

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