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CAS

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1357519-05-1

(2-bromoallyl)(4-nitrophenyl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1357519-05-1 Structure

  • Basic information

    1. Product Name: (2-bromoallyl)(4-nitrophenyl)sulfane
    2. Synonyms: (2-bromoallyl)(4-nitrophenyl)sulfane
    3. CAS NO:1357519-05-1
    4. Molecular Formula:
    5. Molecular Weight: 274.138
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1357519-05-1.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: (2-bromoallyl)(4-nitrophenyl)sulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-bromoallyl)(4-nitrophenyl)sulfane(1357519-05-1)
    11. EPA Substance Registry System: (2-bromoallyl)(4-nitrophenyl)sulfane(1357519-05-1)

  • 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: 1357519-05-1(Hazardous Substances Data)

1357519-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1357519-05-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,5,1 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1357519-05:
(9*1)+(8*3)+(7*5)+(6*7)+(5*5)+(4*1)+(3*9)+(2*0)+(1*5)=171
171 % 10 = 1
So 1357519-05-1 is a valid CAS Registry Number.

1357519-05-1Relevant articles and documents

Highly chemoselective synthesis of aryl allylic sulfoxides through calcium hypobromite oxidation of aryl allylic sulfides

Pace, Vittorio,Castoldi, Laura,Holzer, Wolfgang

, p. 967 - 972 (2012)

A highly chemoselective oxidation of widely substituted aryl allylic sulfides, prepared by allylation of arylthioethers with KF-Celite, to the corresponding aryl allylic sulfoxide was achieved by employing calcium hypobromite. Neither over-oxidation to sulfones nor halogenation of the aromatic rings was observed. The protocol may be successfully applied for the oxidation of substituted allylic systems (i.e., 2-haloallyl) that per se could interact with the oxidizing agent.

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