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CAS

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128864-05-1

2-(2,4-Dimethyl-phenylsulfanylthiocarbonyl)-malonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128864-05-1 Structure

  • Basic information

    1. Product Name: 2-(2,4-Dimethyl-phenylsulfanylthiocarbonyl)-malonic acid diethyl ester
    2. Synonyms:
    3. CAS NO:128864-05-1
    4. Molecular Formula:
    5. Molecular Weight: 340.464
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128864-05-1.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-(2,4-Dimethyl-phenylsulfanylthiocarbonyl)-malonic acid diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,4-Dimethyl-phenylsulfanylthiocarbonyl)-malonic acid diethyl ester(128864-05-1)
    11. EPA Substance Registry System: 2-(2,4-Dimethyl-phenylsulfanylthiocarbonyl)-malonic acid diethyl ester(128864-05-1)

  • 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: 128864-05-1(Hazardous Substances Data)

128864-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128864-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128864-05:
(8*1)+(7*2)+(6*8)+(5*8)+(4*6)+(3*4)+(2*0)+(1*5)=151
151 % 10 = 1
So 128864-05-1 is a valid CAS Registry Number.

128864-05-1Downstream Products

128864-05-1Relevant articles and documents

Cyclization of aromatic dithioic esters: Synthesis of 1,3-benzodithioles

Yeung,Klein

, p. 2121 - 2124 (2007/10/02)

The two step synthesis of 1,3-benzodithiol-2-ylidene compounds such as 4 is described starting from various aromatic thiols 1.

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