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1-(PHENYLSULFONYL)CYCLOPENTANECARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134937-34-1 Structure
  • Basic information

    1. Product Name: 1-(PHENYLSULFONYL)CYCLOPENTANECARBOXYLIC ACID
    2. Synonyms: 1-Benzenesulfonyl-cyclopentanecarboxylic acid;Cyclopentanecarboxylic acid, 1-(phenylsulfonyl)-;1-(benzenesulfonyl)cyclopentane-1-carboxylic acid
    3. CAS NO:134937-34-1
    4. Molecular Formula: C12H14O4S
    5. Molecular Weight: 254.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134937-34-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 487.6°Cat760mmHg
    3. Flash Point: 248.7°C
    4. Appearance: /
    5. Density: 1.362g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.59
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(PHENYLSULFONYL)CYCLOPENTANECARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(PHENYLSULFONYL)CYCLOPENTANECARBOXYLIC ACID(134937-34-1)
    12. EPA Substance Registry System: 1-(PHENYLSULFONYL)CYCLOPENTANECARBOXYLIC ACID(134937-34-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 134937-34-1(Hazardous Substances Data)

134937-34-1 Usage

Appearance

White to off-white crystalline solid

Usage

Synthetic building block in the pharmaceutical industry

Applications

Development of various drugs

Role

Precursor for the synthesis of other organic compounds

Ability

To form stable salts

Potential

As an anti-inflammatory and analgesic agent

Investigation

For its potential role as a substrate in organic chemistry reactions

Value

Valuable compound for research and development in the field of medicinal chemistry and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 134937-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,3 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134937-34:
(8*1)+(7*3)+(6*4)+(5*9)+(4*3)+(3*7)+(2*3)+(1*4)=141
141 % 10 = 1
So 134937-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4S/c13-11(14)12(8-4-5-9-12)17(15,16)10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2,(H,13,14)

134937-34-1SDS

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)cyclopentane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-phenylsulfonylcyclopentanecarboxylic acid

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:134937-34-1 SDS

134937-34-1Downstream Products

134937-34-1Relevant articles and documents

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.

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