112175-38-9

Basic information

• Product Name: Propanamide, N-(4-benzoyl-3-pyridinyl)-2,2-dimethyl-
• CAS NO: 112175-38-9
• Molecular Formula: C17H18N2O2
• Molecular Weight: 282.342
• Mol File: 112175-38-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Propanamide, N-(4-benzoyl-3-pyridinyl)-2,2-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanamide, N-(4-benzoyl-3-pyridinyl)-2,2-dimethyl-(112175-38-9)
• EPA Substance Registry System: Propanamide, N-(4-benzoyl-3-pyridinyl)-2,2-dimethyl-(112175-38-9)

Safety Data

• Hazardous Substances Data: 112175-38-9(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 462-08-8 pyridin-3-ylamine 
• 6919-61-5 N-methoxy-N-methylbenzamide 
• 70298-88-3 N-(pyridin-3-yl)pivalamide 
• 100-52-7 benzaldehyde 
• 82791-70-6 2,2-Dimethyl-N-<4-(hydroxyphenylmethyl)-3-pyridinyl>propanamide 
• 1696-17-9 N,N-diethylbenzamide 

Downstream Products

• 112175-39-0 1,3-dihydro-1-methyl-5-phenyl-2H-pyrido<3,4-e>-1,4-diazepin-2-one 
• 112175-42-5 3-tert-butoxycarbonylaminomethylcarbonylamino-4-benzoylpyridine 
• 15505-59-6 3-benzyloxycarbonylaminomethylcarbonylamino-4-benzoylpyridine 
• 3810-18-2 1,3-dihydro-5-phenyl-2H-pyrido<3,4-e>-1,4-diazepin-2-one 
• 1373774-82-3 4-(1-phenylethenyl)pyridin-3-amine 
• 1373774-90-3 N-[4-(1-phenylethenyl)pyridin-3-yl]formamide 
• 1373774-98-1 3-isocyano-4-(1-phenylethenyl)pyridine 
• 1373775-06-4 4-phenyl-1,7-naphthyridine-2(1H)-thione 
• 125867-45-0 10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine 
• 125867-42-7 4-phenyl-1,2-dihydropyrido<3,4-d>-2-pyrimidinone 
• 3810-11-5 (3-aminopyridin-4-yl)(phenyl)methanone 

Relevant articles and documents

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Provided herein are compounds and pharmaceutical compositions comprising quinolinones. The quinolinones and compositions thereof are useful as eukaryotic translation initiation factor 4F (eIF4F) complex modulators.

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Synthesis of aza analogues of the anticancer agent batracylin

Three series of pyrido-fused pyrimido[2,1-a]isoindol-7-ones were prepared from readily available (aminopyridinyl)(aryl)methanones by reduction followed by a Mitsunobu reaction with phthalimide and acid-catalysed cyclodehydration. This approach provides a wide variety of aza analogues of the antitumour agent batracylin.