147961-58-8

Basic information

• Product Name: tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-carboxymethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate
• Synonyms: tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-carboxymethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate
• CAS NO: 147961-58-8
• Molecular Weight: 490.597
• Mol File: 147961-58-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-carboxymethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-carboxymethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate(147961-58-8)
• EPA Substance Registry System: tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-carboxymethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate(147961-58-8)

Safety Data

• Hazardous Substances Data: 147961-58-8(Hazardous Substances Data)

Upstream product

• 153427-71-5 2,2,2-Trichloroethyl 3-(R)-benzyloxycarbonyloctanoate 
• 147961-55-5 (4S)-4-isopropyl-3-<(2R)-2-(tert-butyloxycarbonylmethyl)-1-oxoheptyl>-2-oxazolidinone 
• 147961-56-6 tert-butyl (3R)-3-benzyloxycarbonyloctanoate 
• 153427-70-4 (3R)-3-benzyloxycarbonyloctanoic acid 
• 147961-57-7 (2R)-2-<(2,2,2-trichloroethoxycarbonyl)methyl>heptanoic acid 
• 145588-98-3 (4S)-4-isopropyl-3-(1-oxoheptyl)-2-oxazolidinone 
• 147983-31-1 tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-1-oxo-2-<(2,2,2-trichloroethoxycarbonyl)methyl>heptyl>hexahydropyridazine-3-carboxylate 

Downstream Products

• 147983-32-2 (3S)-1-benzyloxycarbonyl-2-<(2R)-2-benzyloxyaminocarbonylmethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylic acid 
• 147961-59-9 N-<(1S)-1-<(1S)-1-methylpropyl>-2-oxobutyl>-(3S)-1-benzyloxycarbonyl-2-<(2R)-2-benzyloxyaminocarbonylmethyl-1-oxoheptyl>hexahydropyridazine-3-carboxamide 
• 153744-13-9 N-<(1R)-1-<(1R)-1-methylpropyl>-2-oxobutyl>-(3S)-1-benzyloxycarbonyl-2-<(2R)-2-benzyloxyaminocarbonylmethyl-1-oxoheptyl>hexahydropyridazine-3-carboxamide 
• 147983-33-3 tert-butyl (3S)-1-benzyloxycarbonyl-2-<(2R)-2-benzyloxyaminocarbonylmethyl-1-oxoheptyl>hexahydropyridazine-3-carboxylate 

Relevant articles and documents

Matlystatins, new inhibitors of type IV collagenases from Actinomadura atramentaria. IV. Synthesis and structure-activity relationships of matlystatin B and its stereoisomers

The first total synthesis of matlystatin B (1a), a low molecular weight inhibitor of type IV collagenases, was accomplished, and its absolute configuration was unambiguously determined. Furthermore, ten stereoisomers of 1a were synthesized, and the inhibi