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1307296-49-6

(R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1307296-49-6 Structure

  • Basic information

    1. Product Name: (R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide
    2. Synonyms: (R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide
    3. CAS NO:1307296-49-6
    4. Molecular Formula:
    5. Molecular Weight: 369.915
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1307296-49-6.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: (R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide(1307296-49-6)
    11. EPA Substance Registry System: (R,S)-N-benzyl-N-(1-phenylethyl)-p-chlorobenzenesulfinamide(1307296-49-6)

  • 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: 1307296-49-6(Hazardous Substances Data)

1307296-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1307296-49-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,7,2,9 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1307296-49:
(9*1)+(8*3)+(7*0)+(6*7)+(5*2)+(4*9)+(3*6)+(2*4)+(1*9)=156
156 % 10 = 6
So 1307296-49-6 is a valid CAS Registry Number.

1307296-49-6Relevant articles and documents

Practical and highly stereoselective method for the preparation of several chiral arylsulfinamides and arylsulfinates based on the spontaneous crystallization of diastereomerically pure N-benzyl-N-(1-phenylethyl)- arylsulfinamides

Zhu, Rui-Heng,Shi, Xiao-Xin

, p. 387 - 393 (2011/06/11)

A novel and simple process for the preparation of enantiomerically pure (SS)-benzenesulfinamide (SS)-3a, (SS)-p- toluenesulfinamide (SS)-3b, (SS)-p-chloro- benzenesulfinamide (SS)-3c and (SS)-p- fluorobenzenesulfinamide (SS)-3d has been developed. The treatment of arylsulfinyl chlorides with (R)-N-benzyl-1-phenylethanamine in the presence of excess triethylamine gave diastereomeric mixtures of N-benzyl-N-(1-phenylethyl)- arylsulfinamides 1, which underwent spontaneous crystallization to furnish diastereomerically pure (R,SS)-N-benzyl-N-(1-phenylethyl)- arylsulfinamides (R,SS)-1a-1d in 28%, 29%, 27% and 31% yields, respectively. The diastereomerically pure compounds (R,SS)-1 were then converted into four enantiopure (RS)-methyl arylsulfinates (RS)-2, and finally into four enantiopure (SS)- arylsulfinamides (SS)-3 in good yields.

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