477741-27-8

Basic information

• Product Name: 11-Oxa-2,7,9-triazatridec-7-enoic acid, 3-[2-[[2-[(aminocarbonyl)amino]-1,4,5,6-tetrahydro-4-oxo-5-pyrimidinyl] methylamino]-2-oxoethyl]-8-[[(1,1-dimethylethoxy)carbonyl]amino]-12,12 -dimethyl-10-oxo-9-(2-pyridinylmethyl)-, phenylmethyl ester, (3S)-
• CAS NO: 477741-27-8
• Molecular Formula: C37H52N10O9
• Molecular Weight: 780.881
• Mol File: 477741-27-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 11-Oxa-2,7,9-triazatridec-7-enoic acid, 3-[2-[[2-[(aminocarbonyl)amino]-1,4,5,6-tetrahydro-4-oxo-5-pyrimidinyl] methylamino]-2-oxoethyl]-8-[[(1,1-dimethylethoxy)carbonyl]amino]-12,12 -dimethyl-10-oxo-9-(2-pyridinylmethyl)-, phenylmethyl ester, (3S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 11-Oxa-2,7,9-triazatridec-7-enoic acid, 3-[2-[[2-[(aminocarbonyl)amino]-1,4,5,6-tetrahydro-4-oxo-5-pyrimidinyl] methylamino]-2-oxoethyl]-8-[[(1,1-dimethylethoxy)carbonyl]amino]-12,12 -dimethyl-10-oxo-9-(2-pyridinylmethyl)-, phenylmethyl ester, (3S)-(477741-27-8)
• EPA Substance Registry System: 11-Oxa-2,7,9-triazatridec-7-enoic acid, 3-[2-[[2-[(aminocarbonyl)amino]-1,4,5,6-tetrahydro-4-oxo-5-pyrimidinyl] methylamino]-2-oxoethyl]-8-[[(1,1-dimethylethoxy)carbonyl]amino]-12,12 -dimethyl-10-oxo-9-(2-pyridinylmethyl)-, phenylmethyl ester, (3S)-(477741-27-8)

Safety Data

• Hazardous Substances Data: 477741-27-8(Hazardous Substances Data)

Upstream product

• 586-98-1 2-Hydroxymethylpyridine 
• 468071-40-1 (3'S,5RS)-5-[N-(3-benzyloxycarbonylamino-6-tert-butoxycarbonylamino)hexanoyl-N-methylamino]-5,6-dihydro-2-ureidopyrimid-4(1H)-one 
• 207570-27-2 rac-1,4,5,6-tetrahydro-5-methylamino-2-ureidopyrimidin-4-one 

Relevant articles and documents

Toward a library synthesis of the natural dipeptide antibiotic TAN 1057 A,B

The natural dipeptide antibiotic TAN 1057 A,B represents a promising new antibiotic entity. In this communication we report a novel approach for the synthesis of TAN 1057 A,B analogs bearing variations in the β-arginine side chain. This approach involves a combination of liquid and solid phase methods and allows for a library synthesis of analogs of the natural product.