391594-67-5

Basic information

• Product Name: Heptanedioic acid, 2-hydroxy-6-[[(phenylmethoxy)carbonyl]amino]-, dimethyl ester, (6S)-
• CAS NO: 391594-67-5
• Molecular Formula: C17H23NO7
• Molecular Weight: 353.372
• Mol File: 391594-67-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Heptanedioic acid, 2-hydroxy-6-[[(phenylmethoxy)carbonyl]amino]-, dimethyl ester, (6S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Heptanedioic acid, 2-hydroxy-6-[[(phenylmethoxy)carbonyl]amino]-, dimethyl ester, (6S)-(391594-67-5)
• EPA Substance Registry System: Heptanedioic acid, 2-hydroxy-6-[[(phenylmethoxy)carbonyl]amino]-, dimethyl ester, (6S)-(391594-67-5)

Safety Data

• Hazardous Substances Data: 391594-67-5(Hazardous Substances Data)

Upstream product

• 178859-58-0 (S)-2-Benzyloxycarbonylamino-6-oxo-heptanedioic acid dimethyl ester 
• 78553-51-2 (S)-2-(benzyloxycarbonylamino)pent-4-enoic acid 
• 50299-14-4 N-Acetyl-α-allylglycine 
• 203920-13-2 (S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester 
• 203920-11-0 (2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(2-phenylsulfanyl-allyl)-2,5-dihydro-pyrazine 
• 203920-12-1 (S)-2-Amino-4-phenylsulfanyl-pent-4-enoic acid methyl ester 
• 501-53-1 benzyl chloroformate 
• 78553-47-6 methyl (2S)-2-[N-(benzyloxycarbonyl)amino]pent-4-enoate 
• 50299-15-5 methyl (S)-allylglycinate 
• 16338-48-0 L-allylglycine 

Downstream Products

• 14289-34-0 (S,S)-2,6-diaminopimelic acid 
• 583-93-7 (2R,6S)-2,6-diaminoheptanedioic acid 
• 391594-69-7 (2S)-N-(benzyloxycarbonyl)-1,2,3,4-tetrahydropyridine-2,6-carboxylic acid 
• 391594-68-6 dimethyl (2RS,6S)-2-[N-(benzyloxycarbonyl)-N-(p-tolylsulfonyl)amino]-6-[N-(benzyloxycarbonyl)amino]heptane-1,7-dioate 
• 178859-58-0 (S)-2-Benzyloxycarbonylamino-6-oxo-heptanedioic acid dimethyl ester 

Relevant articles and documents

The first stereospecific synthesis of L-tetrahydrodipicolinic acid; A key intermediate of diaminopimelate metabolism

L-Tetrahydrodipicolinic acid 1, a key intermediate of diaminopimelate metabolism has been prepared in 6 steps and 23% overall yield from L-allylglycine 4. The key step during this synthesis involves a base mediated cyclisation of dimethyl (2RS,6S)-2-[N-(b

Synthesis and evaluation of novel substrates and inhibitors of N-succinyl-LL-diaminopimelate aminotransferase (DAP-AT) from Escherichia coli

N-Succinyl-LL-diaminopimelate aminotransferase (DAP-AT) (EC 2.6.1.17), a key enzyme in the bacterial pathway to L-lysine, was purified to near homogeneity (1500-fold) in five steps from wild type Escherichia coli ATCC 9637. This pyridoxal phosphate (PLP)