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CAS

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1556906-73-0

(2S,3S)-methyl 3-(4-bromophenyl)-3-(4-methylphenylsulfonamido)-2-(phenylthio)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1556906-73-0 Structure

  • Basic information

    1. Product Name: (2S,3S)-methyl 3-(4-bromophenyl)-3-(4-methylphenylsulfonamido)-2-(phenylthio)propanoate
    2. Synonyms:
    3. CAS NO:1556906-73-0
    4. Molecular Formula:
    5. Molecular Weight: 520.468
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1556906-73-0.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: (2S,3S)-methyl 3-(4-bromophenyl)-3-(4-methylphenylsulfonamido)-2-(phenylthio)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-methyl 3-(4-bromophenyl)-3-(4-methylphenylsulfonamido)-2-(phenylthio)propanoate(1556906-73-0)
    11. EPA Substance Registry System: (2S,3S)-methyl 3-(4-bromophenyl)-3-(4-methylphenylsulfonamido)-2-(phenylthio)propanoate(1556906-73-0)

  • 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: 1556906-73-0(Hazardous Substances Data)

1556906-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1556906-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,6,9,0 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1556906-73:
(9*1)+(8*5)+(7*5)+(6*6)+(5*9)+(4*0)+(3*6)+(2*7)+(1*3)=200
200 % 10 = 0
So 1556906-73-0 is a valid CAS Registry Number.

1556906-73-0Downstream Products

1556906-73-0Relevant articles and documents

Isothiourea-catalyzed asymmetric synthesis of β-lactams and β-amino esters from arylacetic acid derivatives and N -sulfonylaldimines

Smith, Siobhan R.,Douglas, James,Prevet, Hugues,Shapland, Peter,Slawin, Alexandra M. Z.,Smith, Andrew D.

, p. 1626 - 1639 (2014)

The isothiourea HBTM-2.1 (5 mol %) catalyzes the asymmetric formal [2 + 2] cycloaddition of both arylacetic acids (following activation with tosyl chloride) and preformed 2-arylacetic anhydrides with N-sulfonylaldimines, generating stereodefined 2,3-diary

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