78314-67-7

Basic information

• Product Name: 5-Benzyloxy-3-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid amide
• CAS NO: 78314-67-7
• Molecular Weight: 406.503
• Mol File: 78314-67-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-Benzyloxy-3-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid amide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Benzyloxy-3-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid amide(78314-67-7)
• EPA Substance Registry System: 5-Benzyloxy-3-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid amide(78314-67-7)

Safety Data

• Hazardous Substances Data: 78314-67-7(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 78314-64-4 2-Amino-5-benzyloxy-3-hydroxy-pentanoic acid 
• 78314-63-3 3-benzyloxypropionaldehyde diethyl acetal 
• 19790-60-4 3-Benzyloxypropanal 
• 51419-59-1 4-methylbenzylsulfonyl chloride 
• 78314-66-6 5-Benzyloxy-3-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid 

Downstream Products

• 78314-68-8 Methanesulfonic acid 3-benzyloxy-1-(carbamoyl-p-tolylmethanesulfonylamino-methyl)-propyl ester 
• 78314-71-3 C₂₁H₂₈N₆O₆S 
• 78314-78-0 C₁₆H₂₃N₅O₇S 
• 78314-76-8 3-tert-Butoxycarbonylamino-5-hydroxy-1-p-tolylmethanesulfonyl-pyrrolidine-2-carboxylic acid methyl ester 
• 78314-75-7 3-tert-Butoxycarbonylamino-5-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid 
• 78332-18-0 3-tert-Butoxycarbonylamino-5-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid methyl ester 
• 78314-70-2 3-amino-5-benzyloxy-2-(p-tolylmethylsulfonylamino)pentanamide 
• 78314-69-9 3-(2-Benzyloxy-ethyl)-1-p-tolylmethanesulfonyl-aziridine-2-carboxylic acid amide 
• 78314-74-6 3-Amino-5-hydroxy-2-p-tolylmethanesulfonylamino-pentanoic acid 
• 78314-73-5 N-(4-Amino-2-oxo-tetrahydro-pyran-3-yl)-C-p-tolyl-methanesulfonamide 

Relevant articles and documents

CHEMICAL STUDIES ON TUBERACTINOMYCIN. XVIII. SYNTHESES OF DL-DIHYDROVIOMYCIDINE AND DL-VIOMYCIDINE

Dihydroviomycidine (2) and viomycidine (3) were guanidino amino acids derived artificially from tuberactidine (1) in peptide antibiotics tuberactinomycin A and B (viomycin).The amino acids 2 and 3 of DL-forms were synthesized from common precursor, threo-