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C17H13N4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1214268-50-4 Structure
  • Basic information

    1. Product Name: C17H13N4
    2. Synonyms:
    3. CAS NO:1214268-50-4
    4. Molecular Formula:
    5. Molecular Weight: 273.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1214268-50-4.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: C17H13N4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H13N4(1214268-50-4)
    11. EPA Substance Registry System: C17H13N4(1214268-50-4)
  • 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: 1214268-50-4(Hazardous Substances Data)

1214268-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1214268-50-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,2,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1214268-50:
(9*1)+(8*2)+(7*1)+(6*4)+(5*2)+(4*6)+(3*8)+(2*5)+(1*0)=124
124 % 10 = 4
So 1214268-50-4 is a valid CAS Registry Number.

1214268-50-4Upstream product

1214268-50-4Downstream Products

1214268-50-4Relevant articles and documents

One-pot synthesis of linearly fused n-heterocyles from their angular analogues and studies of their redox and electrochromic properties

Sinan, Mominul,Ghosh, Kumaresh,Goswami, Sreebrata

, p. 2065 - 2068 (2010)

Chemical Equation Presented In an unusual chemical transformation, the angular heterocyclic compound [1]ClO4, upon reaction with a primary aromatic amine, is transformed to a linear heterocyclic compound 3 via the angular intermediate [2]ClO4 in one pot. Characterization of the compounds was primarily achieved by 1H and 13C NMR and mass spectral data. Analyses of single-crystal X-ray structures of the representative compounds confirmed, their identities. These compounds exhibit notable spectral and redox properties. Their redox behavior is followed by spectral characterization of the electro-generated radicals. Electrochromic properties of the reference compounds are also explored.

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