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CAS

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876069-72-6

Benzenesulfonamide, N-[2,2-bis(ethylthio)ethyl]-4-methyl-N-(3-phenyl-2-propynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 876069-72-6 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, N-[2,2-bis(ethylthio)ethyl]-4-methyl-N-(3-phenyl-2-propynyl)-
    2. Synonyms:
    3. CAS NO:876069-72-6
    4. Molecular Formula: C22H27NO2S3
    5. Molecular Weight: 433.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 876069-72-6.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: Benzenesulfonamide, N-[2,2-bis(ethylthio)ethyl]-4-methyl-N-(3-phenyl-2-propynyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, N-[2,2-bis(ethylthio)ethyl]-4-methyl-N-(3-phenyl-2-propynyl)-(876069-72-6)
    11. EPA Substance Registry System: Benzenesulfonamide, N-[2,2-bis(ethylthio)ethyl]-4-methyl-N-(3-phenyl-2-propynyl)-(876069-72-6)

  • 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: 876069-72-6(Hazardous Substances Data)

876069-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876069-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,0,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 876069-72:
(8*8)+(7*7)+(6*6)+(5*0)+(4*6)+(3*9)+(2*7)+(1*2)=216
216 % 10 = 6
So 876069-72-6 is a valid CAS Registry Number.

876069-72-6Relevant articles and documents

Mercuric chloride and iodide mediated cyclization of tethered alkynedithioacetals as a general route to five- and six-membered rings: Tuning of regioselectivity by alkyne substitution

Biswas, Goutam,Ghorai, Subir,Bhattacharjya, Anup

, p. 313 - 316 (2007/10/03)

Mercuric chloride mediated cyclization of tethered alkynedithioacetals has been established as a general route to five- and six-membered carbocycles and heterocycles. Substitution at the alkyne terminus leads to preferential formation of five-membered rings, whereas unsubstituted alkynedithioacetals give six-membered rings as the major products. Mercuric iodide interrupts the reaction at the intermediate dithioacetal stage.

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