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1-(phenylsulfonyl)cyclopropanecarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97383-41-0

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97383-41-0 Usage

Functional groups

Cyclopropane derivative
Sulfone
Carboxylic acid

Application

Organic synthesis
Pharmaceutical research
Building block for bioactive compounds

Chemical reactivity

Participates in various chemical reactions
Valuable intermediate in organic chemistry

Hazardous properties

Skin and eye irritation
Harmful if ingested or inhaled

Safety precautions

Handle with care, use appropriate protective equipment (gloves, goggles, etc.)

Check Digit Verification of cas no

The CAS Registry Mumber 97383-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97383-41:
(7*9)+(6*7)+(5*3)+(4*8)+(3*3)+(2*4)+(1*1)=170
170 % 10 = 0
So 97383-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O4S/c11-9(12)10(6-7-10)15(13,14)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,12)

97383-41-0SDS

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 1-(benzenesulfonyl)cyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names F0909-0069

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:97383-41-0 SDS

97383-41-0Relevant academic research and scientific papers

SYNTHESIS OF THE NITRILES AND AMIDES OF 1-(ARYLSULFONYL)CYCLOALKANESCARBOXYLIC ACIDS

Neplyuev, V. M.,Bazavova, I. M.,Esipenko, A. N.,Lozinskii, M. O.

, p. 1712 - 1716 (2007/10/02)

1-Arylsulfonylcycloalkanecarbonitriles were synthesized by the cycloalkylation of arylsulfonylacetonitriles by terminal dihalogenoalkanes under the conditions of phase-transfeer catalysis.Hydrolysis of the products gave 11-arylsulfonylcycloalkanecarboxyli

ALKYLATION OF ETHYL ARYLSULFONYLACETATES IN CATALYTIC TWO-PHASE SYSTEM

Ratajczak, Aleksander,Polanski, Jaroslaw

, p. 1963 - 1971 (2007/10/02)

It was found that ethyl arylsulfonylacetates could be easily dialkylated or cyclodialkylated in catalytic two-phase systems with concentrated aqueous sodium hydroxide, undergoing no hydrolysis under the reaction conditions.

A CONVENIENT SYNTHESIS OF PHENYLSULFONYLALKANOIC ACIDS

Ratajczak, Aleksander,Polanski, Jaroslaw

, p. 1271 - 1275 (2007/10/02)

Ethyl phenylsulfonylacetate is alkylated in high yields with alkyl halides in toluene/K2CO3 two-phase system with TEBA (TBAB) as a catalyst.

Synthesis of 1-Phenylsulfonylcyclopropanecarboxylic Acid Derivatives

Takahashi, Masahiko,Suzuki, Hideo,Kata, Yoshimi

, p. 765 - 766 (2007/10/02)

Ethyl phenylsulfonylacetate was treated with 1,2-dibromoethane in the presence of benzyltriethylammonium chloride and alkali to give 1-phenylsulfonylcyclopropanecarboxylic acid, from which the carbonyl chloride, ester, carboxamide, 1,2-diacylhydrazine, ca

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