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68055-33-4

Benzenecarbothioamide, 4-chloro-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68055-33-4 Structure

  • Basic information

    1. Product Name: Benzenecarbothioamide, 4-chloro-N-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:68055-33-4
    4. Molecular Formula: C14H12ClNS
    5. Molecular Weight: 261.775
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68055-33-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenecarbothioamide, 4-chloro-N-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenecarbothioamide, 4-chloro-N-(phenylmethyl)-(68055-33-4)
    11. EPA Substance Registry System: Benzenecarbothioamide, 4-chloro-N-(phenylmethyl)-(68055-33-4)

  • 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: 68055-33-4(Hazardous Substances Data)

68055-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68055-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,5 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68055-33:
(7*6)+(6*8)+(5*0)+(4*5)+(3*5)+(2*3)+(1*3)=134
134 % 10 = 4
So 68055-33-4 is a valid CAS Registry Number.

68055-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-4-chlorobenzenecarbothioamide

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:68055-33-4 SDS

68055-33-4Relevant articles and documents

A multipathway coupled domino strategy: I2-mediated oxidative thionation for direct synthesis of thiobenzamides from miscellaneous substrates

Li, Hong-Zheng,Xue, Wei-Jian,Yin, Guo-Dong,Wu, An-Xin

supporting information, p. 5843 - 5846 (2015/11/02)

An efficient iodine-mediated multipathway coupled domino reaction has been developed for the synthesis of thiobenzamides from benzylamines, benzylamines/aldehydes, and N-alkyl benzylamines under the same reaction conditions. This approach combines two consecutive domino processes in one pot using iodine as the oxidant.

H-β-zeolite catalyzed transamidation of carboxamides, phthalimide, formamides and thioamides with amines under neat conditions

Rao, Sadu Nageswara,Chandra Mohan, Darapaneni,Adimurthy, Subbarayappa

, p. 95313 - 95317 (2015/11/24)

Efficient transamidation of unactivated carboxamides, phthalimides, formamides and thioamides with amines under solvent-free conditions using H-β-zeolite as a green and recyclable heterogeneous catalyst is described. Easy work up, high purity of the products, recyclability and environmentally-friendly nature of the catalyst are the attractive features of the present methodology. This is the first report for the transamidation of thioamides under heterogeneous conditions.

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