102410-44-6

Basic information

• Product Name: 3-Benzyloxy-pyridine-2-carboxylic acid ((3S,6S,15S,16R,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-yl)-amide
• CAS NO: 102410-44-6
• Molecular Weight: 914.028
• Mol File: 102410-44-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Benzyloxy-pyridine-2-carboxylic acid ((3S,6S,15S,16R,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-yl)-amide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Benzyloxy-pyridine-2-carboxylic acid ((3S,6S,15S,16R,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-yl)-amide(102410-44-6)
• EPA Substance Registry System: 3-Benzyloxy-pyridine-2-carboxylic acid ((3S,6S,15S,16R,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-yl)-amide(102410-44-6)

Safety Data

• Hazardous Substances Data: 102410-44-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 23152-29-6 cyclo-(γO)Pec-PhgO-((3'OH)Pic-)Thr-D-Abu-Pro-MePhe-O- 
• 102410-65-1 Fmoc-Phg-OH 
• 102410-59-3 Pic(3-OBzl)-Thr(H-Phg)-D-Abu-Pro-OBu^t 
• 102410-62-8 Pic(3-OBzl)-Thr(Boc-MePhe-4Kps-Phg-)-D-Abu-Pro-OBu^t 
• 102410-55-9 Pic(3-OBzl)-Thr(Fmoc-Phg-)-D-Abu-Pro-OBu^t 
• 102419-80-7 Pic(3-OBzl)-Thr(Fmoc-Phg-)-OH*HCl 
• 102419-79-4 Pic(3-OBzl)-Thr(Fmoc-Phg-)-OBu^t 
• 102410-51-5 H-D-Abu-Pro-OBu^t*TosOH 
• 102410-52-6 Pic(3-OBzl)-Thr-D-Abu-Pro-OBu^t 
• 5603-02-1 Pic(3-OBzl)-OH*HCl 
• 102410-61-7 Boc-MePhe-4Kps-OMe 
• 102429-30-1 Boc-MePhe-4Kps-OH 
• 102410-48-0 Pic(3-OBzl)-Thr-N₂H₃ 

Relevant articles and documents

BENZYLATION OF VIRGINIAMYCIN S1

Treatment of Virginiamycin S1 (VS1) with benzyl bromide in the presence of potassium fluoride in DMF at r.t. resulted in quantitative formation of 1'-N-Bzl-VS1 (1) exempt of 1'-OBzl-VS1 (2).A 27percent conversion of VS1 into 2 however could be achieved by treatment of VS1 with benzyl bromide in DMF at r.t. in the presence of 1,8-bis(dimethylamino)naphthalene as the base.The structure of 1 was confirmed by 1D and 2D NMR spectroscopy.