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CAS

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1609632-93-0

benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609632-93-0 Structure

  • Basic information

    1. Product Name: benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate
    2. Synonyms: benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate
    3. CAS NO:1609632-93-0
    4. Molecular Formula:
    5. Molecular Weight: 734.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609632-93-0.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: benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate(1609632-93-0)
    11. EPA Substance Registry System: benzyl 3,3-bis(N-(3-(4-bromophenyl)prop-2-ynyl)methylsulfonamido)acrylate(1609632-93-0)

  • 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: 1609632-93-0(Hazardous Substances Data)

1609632-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609632-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,6,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609632-93:
(9*1)+(8*6)+(7*0)+(6*9)+(5*6)+(4*3)+(3*2)+(2*9)+(1*3)=180
180 % 10 = 0
So 1609632-93-0 is a valid CAS Registry Number.

1609632-93-0Downstream Products

1609632-93-0Relevant articles and documents

Access to cyclobutene-fused azepines through au-catalyzed cycloisomerization of stable alkyne tethered ketene N,N -acetals

Nayak, Sanatan,Ghosh, Nayan,Sahoo, Akhila K.

, p. 2996 - 2999 (2014)

A base promoted reaction between N-protected propargyl amines and 3-bromopropiolate readily provides an array of novel stable alkyne-tethered ketene N,N-acetals in good yields. A wide range of structurally complex cyclobutene-fused azepine heterocycles are synthesized through the gold-catalyzed intramolecular cycloisomerization of ketene N,N-acetals for the first time. A plausible reaction pathway is deduced on the basis of the 1H NMR studies.

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