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63842-42-2

Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63842-42-2 Structure

  • Basic information

    1. Product Name: Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester
    2. Synonyms: Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester
    3. CAS NO:63842-42-2
    4. Molecular Formula:
    5. Molecular Weight: 344.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63842-42-2.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: Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester(63842-42-2)
    11. EPA Substance Registry System: Dithioglutarsaeure-S,S-bis-(p-tolyl)-ester(63842-42-2)

  • 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: 63842-42-2(Hazardous Substances Data)

63842-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63842-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,4 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63842-42:
(7*6)+(6*3)+(5*8)+(4*4)+(3*2)+(2*4)+(1*2)=132
132 % 10 = 2
So 63842-42-2 is a valid CAS Registry Number.

63842-42-2Downstream Products

63842-42-2Relevant articles and documents

Silica-promoted facile synthesis of thioesters and thioethers: A highly efficient, reusable and environmentally safe solid support

Basu, Basudeb,Paul, Susmita,Nanda, Ashis K.

, p. 767 - 771 (2010)

An efficient, mild and rapid procedure for the acylation and alkylation of aromatic and aliphatic thiols mediated on a silica gel surface at room temperature is described. The protocol allows the protection of thiols under neutral heterogeneous conditions without requiring any bases or Lewis acids, and the silica gel used as the promoter can be recycled for several runs without any loss of activity.

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