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1305306-04-0

C20H17N is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1305306-04-0 Structure

  • Basic information

    1. Product Name: C20H17N
    2. Synonyms: C20H17N
    3. CAS NO:1305306-04-0
    4. Molecular Formula:
    5. Molecular Weight: 271.362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1305306-04-0.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: C20H17N(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H17N(1305306-04-0)
    11. EPA Substance Registry System: C20H17N(1305306-04-0)

  • 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: 1305306-04-0(Hazardous Substances Data)

1305306-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1305306-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,5,3,0 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1305306-04:
(9*1)+(8*3)+(7*0)+(6*5)+(5*3)+(4*0)+(3*6)+(2*0)+(1*4)=100
100 % 10 = 0
So 1305306-04-0 is a valid CAS Registry Number.

1305306-04-0Downstream Products

1305306-04-0Relevant articles and documents

Synthesis of carbazoles by gold(I)-catalyzed carbocyclization of 2-(enynyl)indoles

Praveen, Chandrasekaran,Perumal, Paramasivan Thirumalai

, p. 521 - 524 (2011/04/17)

A new synthetic protocol for carbazoles through gold(I)-catalyzed intramolecular hydroarylation of (Z)-2-(enynyl)indoles was achieved in good yields. The requisite (Z)-2-(enynyl)indoles were synthesized stereoselectively by trimethylgallium-promoted, Z-selective Wittig olefination of N-alkylindole-2-carboxaldehydes with propargyl ylides. Substrates possessing both alkyl as well as aromatic groups are well tolerated under these reaction conditions. Georg Thieme Verlag Stuttgart.

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