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2-Thiazolidinethione, 3-benzoyl-5-methylene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95927-05-2 Structure
  • Basic information

    1. Product Name: 2-Thiazolidinethione, 3-benzoyl-5-methylene-
    2. Synonyms:
    3. CAS NO:95927-05-2
    4. Molecular Formula: C11H9NOS2
    5. Molecular Weight: 235.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95927-05-2.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: 2-Thiazolidinethione, 3-benzoyl-5-methylene-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Thiazolidinethione, 3-benzoyl-5-methylene-(95927-05-2)
    11. EPA Substance Registry System: 2-Thiazolidinethione, 3-benzoyl-5-methylene-(95927-05-2)
  • 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: 95927-05-2(Hazardous Substances Data)

95927-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95927-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,9,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95927-05:
(7*9)+(6*5)+(5*9)+(4*2)+(3*7)+(2*0)+(1*5)=172
172 % 10 = 2
So 95927-05-2 is a valid CAS Registry Number.

95927-05-2Downstream Products

95927-05-2Relevant articles and documents

Alkylation, Acylation, and Carbamoylation Products of 5-Methylene-1,3-thiazolidine-2-thione

Hanefeld, Wolfgang,Bercin, Erdogan

, p. 58 - 64 (2007/10/02)

The reaction product of prop-2-inylamine and carbon disulfide was contrary to earlier results identified as 5-methylene-1,3-thiazolidine-2-thione (3a).This was reacted with alkyl halides, acyl, carbamoyl, and thiocarbamoyl chlorides.The structures of the

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