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501347-05-3

Carbamic acid, [(1S)-1-methyl-3-[(4-methylphenyl)sulfonyl]-2-oxopropyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501347-05-3 Structure

  • Basic information

    1. Product Name: Carbamic acid, [(1S)-1-methyl-3-[(4-methylphenyl)sulfonyl]-2-oxopropyl]-, 1,1-dimethylethyl ester
    2. Synonyms:
    3. CAS NO:501347-05-3
    4. Molecular Formula: C16H23NO5S
    5. Molecular Weight: 341.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501347-05-3.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: Carbamic acid, [(1S)-1-methyl-3-[(4-methylphenyl)sulfonyl]-2-oxopropyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [(1S)-1-methyl-3-[(4-methylphenyl)sulfonyl]-2-oxopropyl]-, 1,1-dimethylethyl ester(501347-05-3)
    11. EPA Substance Registry System: Carbamic acid, [(1S)-1-methyl-3-[(4-methylphenyl)sulfonyl]-2-oxopropyl]-, 1,1-dimethylethyl ester(501347-05-3)

  • 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: 501347-05-3(Hazardous Substances Data)

501347-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501347-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,3,4 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 501347-05:
(8*5)+(7*0)+(6*1)+(5*3)+(4*4)+(3*7)+(2*0)+(1*5)=103
103 % 10 = 3
So 501347-05-3 is a valid CAS Registry Number.

501347-05-3Relevant articles and documents

An intramolecular Michael reaction strategy for the synthesis of 2,6-disubstituted-3-piperidinols

Sengupta, Saumitra,Mondal, Somnath

, p. 7983 - 7986 (2002)

A new synthetic strategy for 2,6-disubstituted-3-hydroxypiperidines via intramolecular Michael reaction of an α-amino-β-hydroxy-δ-acrylate is described. The latter was derived from L-alanine in a few steps via the key intermediacy of an enantiopure γ-amino-β-keto sulfone.

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