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141357-20-2

Ethanone, 1-(4-chlorophenyl)-2-(1,3-dihydro-1-methyl-2H-benzimidazol-2-ylidene)- , (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141357-20-2 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(4-chlorophenyl)-2-(1,3-dihydro-1-methyl-2H-benzimidazol-2-ylidene)- , (E)-
    2. Synonyms:
    3. CAS NO:141357-20-2
    4. Molecular Formula: C16H13ClN2O
    5. Molecular Weight: 284.745
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141357-20-2.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: Ethanone, 1-(4-chlorophenyl)-2-(1,3-dihydro-1-methyl-2H-benzimidazol-2-ylidene)- , (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(4-chlorophenyl)-2-(1,3-dihydro-1-methyl-2H-benzimidazol-2-ylidene)- , (E)-(141357-20-2)
    11. EPA Substance Registry System: Ethanone, 1-(4-chlorophenyl)-2-(1,3-dihydro-1-methyl-2H-benzimidazol-2-ylidene)- , (E)-(141357-20-2)

  • 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: 141357-20-2(Hazardous Substances Data)

141357-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141357-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,5 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141357-20:
(8*1)+(7*4)+(6*1)+(5*3)+(4*5)+(3*7)+(2*2)+(1*0)=102
102 % 10 = 2
So 141357-20-2 is a valid CAS Registry Number.

141357-20-2SDS

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 1-Methyl-2-<(4-chlorobenzoyl)methylene>benzimidazoline

1.2 Other means of identification

Product number -
Other names 1-(4-Chloro-phenyl)-2-[1-methyl-1,3-dihydro-benzoimidazol-(2E)-ylidene]-ethanone

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:141357-20-2 SDS

141357-20-2Downstream Products

141357-20-2Relevant articles and documents

A new route to 3H-1,5-benzodiazepines and heterocyclic ketene animals from benzoyl substituted ketene dithioacetals and diamines

Huang,Wang

, p. 1273 - 1276 (2007/10/02)

Heterocyclic ketene aminals 5 or 3H-1,5-benzodiazepines 4 were obtained from the reaction of benzoyl substituted ketene dithioacetals 1 with various diamines 2. The mechanism of formation of these two different products are discussed.

THE SYNTHESIS AND TAUTOMERIZATION OF KETENE AMINALS WITH BENZIMIDAZOLINE RING

Huang, Zhi-Tang,Wang, Mei-Xiang

, p. 2325 - 2332 (2007/10/02)

The first isolation of benzimidazoline ring substituted ketene aminals 7a-c and/or their amidine tautomers 7'b-d, which were synthesized by the reactions: (1) benzoyl substituted ketene mercaptals 3 with N-methyl-o-phenylenediamine 4, and (2) 1,2-dimethylbenzimidazole 5 with ethyl benzoates 6, were disclosed.The tautomeric equilibrium between 7 and 7', along with benzothiazoline and benzoxazoline ring substituted ketene N,S-acetals 8 and 8' and ketene N,O-acetals 9 and 9', were discussed.

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