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76664-73-8

4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76664-73-8 Structure

  • Basic information

    1. Product Name: 4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide
    2. Synonyms: 4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide
    3. CAS NO:76664-73-8
    4. Molecular Formula:
    5. Molecular Weight: 347.459
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76664-73-8.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: 4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide(76664-73-8)
    11. EPA Substance Registry System: 4-Methyl-N-[2-(2-methyl-acryloyl)-phenylsulfanyl]-benzenesulfonamide(76664-73-8)

  • 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: 76664-73-8(Hazardous Substances Data)

76664-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76664-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,6 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76664-73:
(7*7)+(6*6)+(5*6)+(4*6)+(3*4)+(2*7)+(1*3)=168
168 % 10 = 8
So 76664-73-8 is a valid CAS Registry Number.

76664-73-8Relevant articles and documents

SULFILIMINES IN ORGANIC SYNTHESES: NEW ENTRIES INTO TETRAHYDRO-1,2-BENZOTHIAZEPINE AND 1,2-BENZISOTHIAZOLE SYSTEMS

Tamura, Yasumitsu,Bayomi, Said M.,Mukai, Chisato,Ikeda, Masazumi,Murase, Masao,Kise, Masahiro

, p. 533 - 536 (2007/10/02)

Novel ring transformations of thiochroman-4-ones and benzothiophen-3(2H)-ones to tetrahydro-1,2-benzothiazepin-5-ones and 1,2-benzisothiazoles via sulfilimine intermediates are described.

Novel Conversions of Benzothiophen-3(2H)-ones into 1,2-Benzisothiasole and Tetrahydro-1,2-benzothiazepin-5-one Systems via Sulphimide Intermediates

Tamura, Yasumitsu,Bayomi, Said M. M.,Mukai, Chisato,Ikeda, Masazumi,Kise, Masahiro

, p. 2830 - 2834 (2007/10/02)

S-Amination of 2,2-dimethyl- (3a) and 2-benzyl-2-methyl-benzothiophen-3(2H)-one (3b) with O-mesitylenesulphonylhydroxylamine followed by treatment with base yielded 3-isopropenyl- (4a) and 3-(1-benzylvinyl)-1,2-benzisothiazole (4b), respectively.Simila

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