40107-91-3

Basic information

• Product Name: 4-CHLORO-6-METHYL-2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE
• Synonyms: 4-CHLORO-6-METHYL-2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE
• CAS NO: 40107-91-3
• Molecular Formula: C₈H₅ClN₂O₂
• Molecular Weight: 196.59
• Mol File: 40107-91-3.mol

Chemical Properties

• Appearance: /
• Density: 1.523±0.06 g/cm3(Predicted)
• PKA: 7.40±0.20(Predicted)
• CAS DataBase Reference: 4-CHLORO-6-METHYL-2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-6-METHYL-2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE(40107-91-3)
• EPA Substance Registry System: 4-CHLORO-6-METHYL-2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE(40107-91-3)

Safety Data

• Hazardous Substances Data: 40107-91-3(Hazardous Substances Data)

Upstream product

• 40108-12-1 ethyl 2-chloro-3-cyano-6-methyl-4-pyridine carboxylate 
• 18619-97-1 ethyl 3-cyano-2-hydroxy-6-methylisonicotinate 

Downstream Products

• 1531587-53-7 C₁₄H₉ClN₂O₂ 
• 1531587-62-8 C₂₀H₁₄ClN₃O₅S 
• 1531587-78-6 C₂₃H₂₀ClN₃O₄S₂ 
• 1531587-79-7 C₂₄H₂₂ClN₃O₄S₂ 
• 1531587-81-1 C₂₄H₂₃ClN₄O₄S 
• 1531587-74-2 C₂₃H₂₀ClN₃O₅S 
• 1531587-75-3 C₂₄H₂₀ClN₃O₄ 
• 1531587-68-4 C₂₄H₂₂ClN₃O₅S 
• 1531587-69-5 C₂₄H₂₂ClN₃O₅S 
• 1531587-70-8 C₂₃H₁₉Cl₂N₃O₅S 
• 1531587-71-9 C₂₃H₁₉ClFN₃O₅S 
• 1531587-72-0 C₂₃H₁₉ClFN₃O₅S 
• 1531587-73-1 C₂₃H₁₉ClFN₃O₅S 
• 1531587-61-7 C₂₃H₁₈ClN₃O₅S 

Relevant articles and documents

Discovery and optimization of N-(3-(1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c] pyridin-4-yloxy)phenyl)benzenesulfonamides as novel GPR119 agonists

The discovery and optimization of novel N-(3-(1,3-dioxo-2,3-dihydro-1H- pyrrolo[3,4-c]pyridin-4-yloxy)phenyl)benzenesulfonamide GPR119 agonists is described. Modification of the pyridylphthalimide motif of the molecule with R1 =-Me and R2 =-iPr substituents, incorporated with a 6-fluoro substitution on the central phenyl ring offered a potent and metabolically stable tool compound 22.

Investigations on the synthesis and properties of some N-arylpiperazinylalkyl derivatives of imides of 3,4-pyridinedicarboxylic acids

The synthesis of N-arylpiperazinylalkyl derivatives of imides of 3,4-pyridinedicarboxylic acid is described. In pharmacological screening some of the obtained compounds displayed biological activity, but they were inactive as anxiolytic agents.