102267-93-6

Basic information

• Product Name: 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione, 3-methyl-6-phenyl-
• CAS NO: 102267-93-6
• Molecular Formula: C14H10N2O2
• Molecular Weight: 238.246
• Mol File: 102267-93-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione, 3-methyl-6-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione, 3-methyl-6-phenyl-(102267-93-6)
• EPA Substance Registry System: 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione, 3-methyl-6-phenyl-(102267-93-6)

Safety Data

• Hazardous Substances Data: 102267-93-6(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 5077-73-6 2,4-dinitrophenylhydrazone of methacrolein 
• 42595-16-4 3-chloro-1-phenyl-1H-pyrrole-2,5-dione 
• 66064-57-1 (E)-1,1-dimethyl-2-(2-methylallylidene)hydrazine 
• 133392-42-4 methacrolein N-methyl-N-(pent-4-ynoyl)hydrazone 
• 138842-30-5 methacrolein N-allyloxycarbonyl-N-methylhydrazone 
• 133392-41-3 1,7-dimethyl-4,4a,5,6-tetrahydropyrido-1H-<1,2-b>pyridazin-2(3H)-one 
• 133392-46-8 methacrolein benzoylhydrazone 
• 133392-42-4 Pent-4-ynoic acid N-methyl-N'-[2-methyl-prop-2-en-(E)-ylidene]-hydrazide 
• 99067-85-3 methacrolein phenylhydrazone 

Relevant articles and documents

Diels-Alder reactions of N-silyloxy 1-azadienes

Novel 1-(t-butyldimethyisilyloxy)-1-aza-1,3-butadienes 1 and 2 are prepared by the reaction of O-(t-butyldimethylsilyloxy)hydroxylamine with methyl vinyl ketone and methacrolein, respectively. Azadienes 1 and 2 through sharing of oxygen nonbonding electrons are activated and thus their Diels-Alder reactions with a number of halobenzoquinones, napthoquinones and N-phenylmaleimide regiospecifically give low to good yields of various pyridine heterocycles.

Process for the preparation of 2,3-pyridinedicarboximides

There is provided a process for the preparation of 2,3-pyridinedicarboximides having the structural formula I The 2,3-pyridinedicarboximides are useful as intermediates in the preparation of herbicidal 2-(2-imidazolin-2-yl)nicotinic acids,

Diels-Alder cycloaddition reactions of αβ-unsaturated aldehyde acylhydrazones

Acylhydrazones derived from N-methyl-N-pent-4-enoylhydrazine or N-methyl-N-pent-4-ynoylhydrazine and αβ-unsaturated aldehydes undergo intramolecular Diels-Aldler reactions at elevated temperatures. An intermolecular counterpart, the addition of methacrole