1359711-06-0

Basic information

• Product Name: 1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester
• Synonyms: 1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester
• CAS NO: 1359711-06-0
• Molecular Weight: 275.304
• Mol File: 1359711-06-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester(1359711-06-0)
• EPA Substance Registry System: 1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester(1359711-06-0)

Safety Data

• Hazardous Substances Data: 1359711-06-0(Hazardous Substances Data)

Upstream product

• 180609-56-7 1-benzoxycarbonyl-2-methoxycarbonylpiperidine 
• 82830-85-1 methyl 6-{[(benzyloxy)carbonyl]amino}-2-diazohexanoate 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 

Downstream Products

• 1359711-07-1 C₁₅H₁₆BrNO₄ 
• 1359711-08-2 1-benzyl 2-methyl 4-hydroxy-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-09-3 1-benzyl 2-methyl (S)-4-hydroxy-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-11-7 1-benzyl 2-methyl (R)-4-hydroxy-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-10-6 1-benzyl 2-methyl (R)-4-(butyryloxy)-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-13-9 2-benzyl 1-methyl (1R,5R,6S)-5-hydroxy-2-azabicyclo[4.1.0]heptane-1,2-dicarboxylate 
• 1359711-14-0 2-benzyl 1-methyl (1S,5S,6R)-5-hydroxy-2-azabicyclo[4.1.0]heptane-1,2-dicarboxylate 
• 1359711-15-1 1-benzyl 2-methyl (R)-4-(tert-butyldimethylsilanyloxy)-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-16-2 1-benzyl 2-methyl (S)-4-(tert-butyldimethylsilanyloxy)-5,6-dihydropyridine-1,2(4H)-dicarboxylate 
• 1359711-20-8 C₂₂H₃₃NO₅Si 

Relevant articles and documents

Synthesis of cis- and trans-(±)-3-mercaptoproline and pipecolic acid derivatives via thio-Michael addition

The reactivity of 2,3-dehydroproline and 2,3-dehydropipecolic acid methyl ester derivatives with S-nucleophiles in the thio-Michael addition reaction has been explored. The addition of triphenylmethanethiol and subsequent trityl cleavage led to the corres

Diastereodivergent synthesis of 4-hydroxy-2,3-methanopipecolic acid derivatives as conformationally constrained homoserine analogues

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