706778-81-6

Basic information

• Product Name: N-benzyloxy-N-[(2R)-cyclopentylmethyl-3-oxo-3-(tetrahydropyridazin-1-yl)propyl]formamide
• Synonyms: N-benzyloxy-N-[(2R)-cyclopentylmethyl-3-oxo-3-(tetrahydropyridazin-1-yl)propyl]formamide
• CAS NO: 706778-81-6
• Molecular Weight: 373.495
• Mol File: 706778-81-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-benzyloxy-N-[(2R)-cyclopentylmethyl-3-oxo-3-(tetrahydropyridazin-1-yl)propyl]formamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyloxy-N-[(2R)-cyclopentylmethyl-3-oxo-3-(tetrahydropyridazin-1-yl)propyl]formamide(706778-81-6)
• EPA Substance Registry System: N-benzyloxy-N-[(2R)-cyclopentylmethyl-3-oxo-3-(tetrahydropyridazin-1-yl)propyl]formamide(706778-81-6)

Safety Data

• Hazardous Substances Data: 706778-81-6(Hazardous Substances Data)

Upstream product

• 89990-53-4 1,2,3,4,5,6-hexahydropyridazine hydrochloride 
• 301684-75-3 (2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoic acid 
• 1316663-23-6 C₂₆H₃₉N₃O₅ 
• 89990-53-4 tetrahydropyridazine dihydrochloride 

Downstream Products

• 706778-84-9 2-[3-(benzyloxyformylamino)-(2R)-cyclopentylmethyl-propionyl]-tetrahydropyridazine-1-carboxylic acid methylphenylamide 
• 706778-82-7 N-benzyloxy-N-{(2R)-cyclopentylmethyl-3-[2-(furan-2-carbonyl)-tetrahydropyridazin-1-yl]-3-oxo-propyl}formamide 
• 706778-40-7 N-{(2R)-cyclopentylmethyl-3-[2-cyclohexanecarbonyl-tetrahydropyridazin-1-yl]-3-oxo-propyl}-N-hydroxyformamide 
• 706778-37-2 N-{(2R)-cyclopentylmethyl-3-[2-benzoyl-tetrahydropyridazin-1-yl]-3-oxo-propyl}-N-hydroxyformamide 
• 706778-41-8 N-{(2R)-cyclopentylmethyl-3-[2-(4-methoxybenzoyl)-tetrahydropyridazin-1-yl]-3-oxo-propyl}-N-hydroxyformamide 
• 706778-44-1 N-{(2R)-cyclopentylmethyl-3-[2-(4-fluorobenzoyl)-tetrahydropyridazin-1-yl]-3-oxo-propyl}-N-hydroxyformamide 

Relevant articles and documents

Peptidomimetic inhibitors of bacterial peptide deformylase

A series of N-formyl hydroxylamine peptide deformylase inhibitors containing a cyclic azaamino acid moiety between the P1′ and P3′ substituents are presented. Selected compounds display antibacterial activity against pathogens associated with respiratory