104910-79-4

• 

• Basic information

  1. Product Name: Quinoxaline, 2-ethenyl-3-methyl-
  2. Synonyms: Quinoxaline, 2-ethenyl-3-methyl-
  3. CAS NO:104910-79-4
  4. Molecular Formula: C11H10N2
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 104910-79-4.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Quinoxaline, 2-ethenyl-3-methyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Quinoxaline, 2-ethenyl-3-methyl-(104910-79-4)
  11. EPA Substance Registry System: Quinoxaline, 2-ethenyl-3-methyl-(104910-79-4)

• 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: 104910-79-4(Hazardous Substances Data)

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104910-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104910-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,1 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104910-79:
(8*1)+(7*0)+(6*4)+(5*9)+(4*1)+(3*0)+(2*7)+(1*9)=104
104 % 10 = 4
So 104910-79-4 is a valid CAS Registry Number.

104910-79-4Upstream product

• 1131-47-1 2,4-dimethyl-6,7-benzo-1,5-diazepine 

104910-79-4Downstream Products

104910-79-4Relevant articles and documents

Flash vacuum pyrolysis of 1,5-benzodiazepines

Despinoy, Christophe,Lloyd, Douglas,McNab, Hamish,Reed, David

, p. 9667 - 9676 (1998)

Gas-phase pyrolysis of the 2,4-diphenyl- and 2,4-dimethyl-1,5- benzodiazepines 3 and 4 at 800-850 °C gave a range of heterocyclic products (e.g. quinoxalines 8, 10 and 11, indole 9, benzimidazole 5 and pyrazole 7) in low yields. The formation of most products is initiated by cleavage of the 2,3-bond to give a diradical intermediate, though the pyrazole is obtained by a mechanism involving a 1,5-hydrogen shift followed by an unusual ring contraction.

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