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138850-14-3

Benzenesulfinamide, N-[2-(1-cyclohexen-1-yl)phenyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138850-14-3 Structure

  • Basic information

    1. Product Name: Benzenesulfinamide, N-[2-(1-cyclohexen-1-yl)phenyl]-4-methyl-
    2. Synonyms:
    3. CAS NO:138850-14-3
    4. Molecular Formula: C19H21NOS
    5. Molecular Weight: 311.448
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138850-14-3.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: Benzenesulfinamide, N-[2-(1-cyclohexen-1-yl)phenyl]-4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfinamide, N-[2-(1-cyclohexen-1-yl)phenyl]-4-methyl-(138850-14-3)
    11. EPA Substance Registry System: Benzenesulfinamide, N-[2-(1-cyclohexen-1-yl)phenyl]-4-methyl-(138850-14-3)

  • 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: 138850-14-3(Hazardous Substances Data)

138850-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138850-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138850-14:
(8*1)+(7*3)+(6*8)+(5*8)+(4*5)+(3*0)+(2*1)+(1*4)=143
143 % 10 = 3
So 138850-14-3 is a valid CAS Registry Number.

138850-14-3Relevant articles and documents

The conversion of benzothiazines to 2-alkenyl anilines

Harmata,Herron

, p. 8855 - 8862 (2007/10/02)

Upon treatment with excess potassium dimsylate in DMSO benzothiazines 1a-1j undergo an elimination of the sulfoximine functional group to give 2-alkenylsulfinanilides nonstereoselectively in good to excellent yield. These are easily converted to the corre

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