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Technology Process of Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-

Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-

Base Information
  • Chemical Name:Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-
  • CAS No.:6687-74-7
  • Molecular Formula:C16H18N2O2
  • Molecular Weight:270.3263
  • Hs Code.:2933990090
  • NSC Number:79482
  • DSSTox Substance ID:DTXSID10217001
  • Nikkaji Number:J48.374E
  • Wikidata:Q83093367
  • Mol file:6687-74-7.mol
Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-

Synonyms:6687-74-7;Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-;1-(6,7-dimethyl-4-prop-2-enoyl-2,3-dihydroquinoxalin-1-yl)prop-2-en-1-one;NSC 79482;BRN 0924580;5-23-06-00094 (Beilstein Handbook Reference);NSC79482;1,4-Diacryloyl-6,7-dimethyl-1,2,3,4-tetrahydroquinoxaline;Quinoxaline, 1,4-diacryloyl-1,2,3,4-tetrahydro-6,7-dimethyl-;Quinoxaline, 1,2,3,4-tetrahydro-6,7-dimethyl-1,4-bis(1-oxo-2-propenyl)-;DTXSID10217001;1,4-Diacryloyl-1,2,3,4-tetrahydro-6,7-dimethylquinoxaline;NSC-79482;WLN: T66 BN ENT&J BV1U1 EV1U1 H1 I1;Quinoxaline,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-;Quinoxaline,4-diacryloyl-1,2,3,4-tetrahydro-6,7-dimethyl-;Quinoxaline,2,3,4-tetrahydro-6,7-dimethyl-1,4-bis(1-oxo-2-propenyl)-

Suppliers and Price of Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-
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The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of Quinoxaline, 1,2,3,4-tetrahydro-1,4-diacryloyl-6,7-dimethyl-
Chemical Property:
  • Boiling Point:405.4°Cat760mmHg 
  • Flash Point:172.1°C 
  • PSA：40.62000 
  • Density:1.142g/cm3 
  • LogP:2.48500 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:270.136827821
  • Heavy Atom Count:20
  • Complexity:392
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC2=C(C=C1C)N(CCN2C(=O)C=C)C(=O)C=C
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