837410-99-8

Basic information

• Product Name: 2-Pyridinecarboxylic acid, 6-methoxy-5-[[(phenylmethoxy)carbonyl]amino]-, methyl ester
• CAS NO: 837410-99-8
• Molecular Formula: C16H16N2O5
• Molecular Weight: 316.313
• Mol File: 837410-99-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Pyridinecarboxylic acid, 6-methoxy-5-[[(phenylmethoxy)carbonyl]amino]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyridinecarboxylic acid, 6-methoxy-5-[[(phenylmethoxy)carbonyl]amino]-, methyl ester(837410-99-8)
• EPA Substance Registry System: 2-Pyridinecarboxylic acid, 6-methoxy-5-[[(phenylmethoxy)carbonyl]amino]-, methyl ester(837410-99-8)

Safety Data

• Hazardous Substances Data: 837410-99-8(Hazardous Substances Data)

Upstream product

• 837410-85-2 methyl (5S,2Z)-4-(3-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl)-2-t-butoxycarbonylamino-2-butenoate 
• 837410-88-5 methyl (5S,2Z)-5-benzyloxycarbonylamino-2-t-butoxycarbonylamino-6-hydroxy-2-hexenoate 
• 837410-93-2 methyl (5S)-5-benzyloxycarbonylamino-6-oxo-1-t-butoxycarbonyl-4,5,6-trihydropyridine-2-carboxylate 
• 837410-90-9 methyl (6RS,5S)-5-benzyloxycarbonylamino-6-hydroxy-1-t-butoxycarbonyl-4,5,6-trihydropyridine-2-carboxylate 
• 837410-95-4 methyl (5S)-5-benzyloxycarbonylamino-6-oxo-1,4,5-trihydropyridine-2-carboxylate 
• 837410-82-9 methyl (4S)-(3-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-y)acetate 
• 607376-66-9 2-[(4S)-(3-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-y)]ethanol 
• 607376-67-0 (S)-2,2-dimethyl-4-(2-oxo-ethyl)-oxazolidine-3-carboxylic acid benzyl ester 
• 192517-47-8 methyl (3S)-3-[[(benzyloxy)carbonyl]amino]-4-hydroxybutanoate 
• 3160-47-2 N-(benzyloxycarbonyl)-L-aspartic acid 4-methyl ester 
• 74-88-4 methyl iodide 
• 837410-97-6 methyl 5-benzyloxycarbonylamino-6-oxo-1-hydropyridine-2-carboxylate 

Downstream Products

• 475272-68-5 methyl 5-amino-6-methoxypyridine-2-carboxylate 

Relevant articles and documents

Useful synthesis of 2,3,6-tri- and 2,3,5,6-tetrasubstitutedpyridine derivatives from aspartic acid

New synthetic methods for 2,3,6-tri- and 2,3,5,6-tetrasubstituted pyridineskeletons, which are the essential main central segments of thiostrepton-type macrocyclic antibiotics, were developed from l-α-aspartic acid (Asp) via the Asp-derived α-dehydroamino