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3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1423039-54-6 Structure
  • Basic information

    1. Product Name: 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile
    2. Synonyms: 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile
    3. CAS NO:1423039-54-6
    4. Molecular Formula:
    5. Molecular Weight: 312.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1423039-54-6.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: 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile(1423039-54-6)
    11. EPA Substance Registry System: 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile(1423039-54-6)
  • 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: 1423039-54-6(Hazardous Substances Data)

1423039-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423039-54-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,0,3 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1423039-54:
(9*1)+(8*4)+(7*2)+(6*3)+(5*0)+(4*3)+(3*9)+(2*5)+(1*4)=126
126 % 10 = 6
So 1423039-54-6 is a valid CAS Registry Number.

1423039-54-6Downstream Products

1423039-54-6Relevant articles and documents

Palladium catalyzed decarboxylative rearrangement of N-alloc indoles

Chen, Jun,Cook, Matthew J.

, p. 1088 - 1091 (2013/04/10)

A highly efficient palladium catalyzed decarboxylative allylic rearrangement of alloc indoles has been developed. This can also be combined with a Suzuki-Miyaura cross-coupling reaction in a single pot transformation. Substituted alloc groups and benzylic variants have also been demonstrated alongside promising initial results on the enantioselective variant.

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