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1312681-05-2

(S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312681-05-2 Structure

  • Basic information

    1. Product Name: (S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-methylbenzenesulfonamide
    2. Synonyms:
    3. CAS NO:1312681-05-2
    4. Molecular Formula:
    5. Molecular Weight: 357.517
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312681-05-2.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: (S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-methylbenzenesulfonamide(1312681-05-2)
    11. EPA Substance Registry System: (S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-methylbenzenesulfonamide(1312681-05-2)

  • 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: 1312681-05-2(Hazardous Substances Data)

1312681-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312681-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,6,8 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1312681-05:
(9*1)+(8*3)+(7*1)+(6*2)+(5*6)+(4*8)+(3*1)+(2*0)+(1*5)=122
122 % 10 = 2
So 1312681-05-2 is a valid CAS Registry Number.

1312681-05-2Upstream product

1312681-05-2Downstream Products

1312681-05-2Relevant articles and documents

Catalytic asymmetric C-H insertions of rhodium(II) azavinyl carbenes

Chuprakov, Stepan,Malik, Jamal A.,Zibinsky, Mikhail,Fokin, Valery V.

, p. 10352 - 10355 (2011)

A highly efficient enantioselective C-H insertion of azavinyl carbenes into unactivated alkanes has been developed. These transition metal carbenes are directly generated from readily available and stable 1-sulfonyl-1,2,3-triazoles in the presence of chiral Rh(II) carboxylates and are used for C-H functionalization of alkanes to access a variety of β-chiral sulfonamides.

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