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CAS

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1384881-78-0

2,2-bis(4(methylthio)phenyl)pent-4-penenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384881-78-0 Structure

  • Basic information

    1. Product Name: 2,2-bis(4(methylthio)phenyl)pent-4-penenitrile
    2. Synonyms:
    3. CAS NO:1384881-78-0
    4. Molecular Formula:
    5. Molecular Weight: 325.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384881-78-0.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: 2,2-bis(4(methylthio)phenyl)pent-4-penenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-bis(4(methylthio)phenyl)pent-4-penenitrile(1384881-78-0)
    11. EPA Substance Registry System: 2,2-bis(4(methylthio)phenyl)pent-4-penenitrile(1384881-78-0)

  • 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: 1384881-78-0(Hazardous Substances Data)

1384881-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384881-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,8,8 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1384881-78:
(9*1)+(8*3)+(7*8)+(6*4)+(5*8)+(4*8)+(3*1)+(2*7)+(1*8)=210
210 % 10 = 0
So 1384881-78-0 is a valid CAS Registry Number.

1384881-78-0Relevant articles and documents

6-azabicyclo[3.2.1]octanes via copper-catalyzed enantioselective alkene carboamination

Casavant, Barbara J.,Hosseini, Azade S.,Chemler, Sherry R.

, p. 2697 - 2702 (2014)

Bridged bicyclic rings containing nitrogen heterocycles are important motifs in bioactive small organic molecules. An enantioselective copper-catalyzed alkene carboamination reaction that creates bridged heterocycles is reported herein. Two new rings are

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