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CAS

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1213779-01-1

methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1213779-01-1 Structure

  • Basic information

    1. Product Name: methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate
    2. Synonyms: methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate
    3. CAS NO:1213779-01-1
    4. Molecular Formula:
    5. Molecular Weight: 359.446
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1213779-01-1.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: methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate(1213779-01-1)
    11. EPA Substance Registry System: methyl (2S)-allyl(4-methylphenylsulfonyl)amino(phenyl)acetate(1213779-01-1)

  • 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: 1213779-01-1(Hazardous Substances Data)

1213779-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1213779-01-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,7,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1213779-01:
(9*1)+(8*2)+(7*1)+(6*3)+(5*7)+(4*7)+(3*9)+(2*0)+(1*1)=141
141 % 10 = 1
So 1213779-01-1 is a valid CAS Registry Number.

1213779-01-1Relevant articles and documents

Concise total asymmetric synthesis of (S)-2-phenylpiperidin-3-one

Gaucher, Xavier,Jida, Mouhamad,Ollivier, Jean

, p. 3320 - 3322 (2009)

Starting from readily available dihydropyridinones, we have developed the first synthesis of (S)-2-phenylpiperidin-3-one. While the scaffold appears relatively common, even in its racemic form, this original product can be considered as a potential precur

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