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78605-16-0

2-Methyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78605-16-0 Structure

  • Basic information

    1. Product Name: 2-Methyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine
    2. Synonyms:
    3. CAS NO:78605-16-0
    4. Molecular Formula:
    5. Molecular Weight: 209.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78605-16-0.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-Methyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine(78605-16-0)
    11. EPA Substance Registry System: 2-Methyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine(78605-16-0)

  • 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: 78605-16-0(Hazardous Substances Data)

78605-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78605-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,0 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78605-16:
(7*7)+(6*8)+(5*6)+(4*0)+(3*5)+(2*1)+(1*6)=150
150 % 10 = 0
So 78605-16-0 is a valid CAS Registry Number.

78605-16-0Downstream Products

78605-16-0Relevant articles and documents

Cyclisation par amination intramoleculaire dans la serie de la pyrazine.

Vierfond, Jean-Michel,Mettey, Yvette,Mascrier-Demagny, Line,Miocque, Marcel

, p. 1219 - 1222 (2007/10/02)

An original one-pot synthesis of 4,7-diazaindoles is achieved by metalation of methylpyrazines or methylquinoxaline which are then condensed with an aromatic nitrile : an intermediate imine-enamine is formed which leads, by intramolecular cyclization, to diazaindoles.

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