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CAS

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76579-53-8

2-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76579-53-8 Structure

  • Basic information

    1. Product Name: 2-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide
    2. Synonyms: 2-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide
    3. CAS NO:76579-53-8
    4. Molecular Formula:
    5. Molecular Weight: 239.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76579-53-8.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-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide(76579-53-8)
    11. EPA Substance Registry System: 2-(3,4-dimethoxyphenyl)-N,N-dimethylethanethioamide(76579-53-8)

  • 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: 76579-53-8(Hazardous Substances Data)

76579-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76579-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76579-53:
(7*7)+(6*6)+(5*5)+(4*7)+(3*9)+(2*5)+(1*3)=178
178 % 10 = 8
So 76579-53-8 is a valid CAS Registry Number.

76579-53-8Relevant articles and documents

The thioamidation ofgem-dibromoalkenes in an aqueous medium

Vankar, Jigarkumar K.,Gupta, Ankush,Jadav, Jaydeepbhai P.,Nanjegowda, Shankara H.,Gururaja, Guddeangadi N.

, p. 2473 - 2480 (2021/04/02)

The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium. The presented green protocol emphasizes the suitability of aqueous media for the thioamidation reaction and enables greater selectivity with synthetic utility. A wide range of thioamides in moderate to excellent yields has been achieved using readily available starting materials, with the use of no organic solvents, catalysts, or additives.

Copper(II)-catalyzed reactions of dimethylformamide with phenylacetonitrile and sulfur to form N,N-dimethylthioamides

Qu, Yanyang,Li, Zhengkai,Xiang, Haifeng,Zhou, Xiangge

supporting information, p. 3141 - 3146 (2013/12/04)

Novel copper-catalyzed three-component reactions of phenylacetonitrile, sulfur and DMF (dimethyformamide) for the selective preparation of N,N-dimethylthiobenzamide and N,N-dimethyl-2-phenylethanethioamides in yields of up to 96% are described. Copyright

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