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1137737-38-2

1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1137737-38-2 Structure

  • Basic information

    1. Product Name: 1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene
    2. Synonyms: 1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene
    3. CAS NO:1137737-38-2
    4. Molecular Formula:
    5. Molecular Weight: 406.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1137737-38-2.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: 1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene(1137737-38-2)
    11. EPA Substance Registry System: 1,1-dibromo-3-hexylsulfanyl-4-methyl-pent-1-ene(1137737-38-2)

  • 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: 1137737-38-2(Hazardous Substances Data)

1137737-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1137737-38-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,7,7,3 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1137737-38:
(9*1)+(8*1)+(7*3)+(6*7)+(5*7)+(4*3)+(3*7)+(2*3)+(1*8)=162
162 % 10 = 2
So 1137737-38-2 is a valid CAS Registry Number.

1137737-38-2Downstream Products

1137737-38-2Relevant articles and documents

Enantioselective synthesis of allenamides via sulfimide [2,3]-sigmatropic rearrangement

Armstrong, Alan,Emmerson, Daniel P.G.

supporting information; experimental part, p. 1547 - 1550 (2009/09/06)

Chiral allenamides are prepared with high levels of enantiomeric purity by [2,3]-sigmatropic rearrangement of propargylic sulfimides. The required branched propargylic sulfides are prepared by an enantioselective organocatalytic aldehyde α-sulfenylation followed by Corey-Fuchs alkynylation.

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