672307-41-4

Basic information

• Product Name: 1(2H)-Pyridazinecarboxylic acid, tetrahydro-3-[[(4S)-2-oxo-4-(phenylmethyl)-3-oxazolidinyl]carbonyl]-, phenylmethyl ester, (3S)-
• CAS NO: 672307-41-4
• Molecular Formula: C23H25N3O5
• Molecular Weight: 423.469
• Mol File: 672307-41-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1(2H)-Pyridazinecarboxylic acid, tetrahydro-3-[[(4S)-2-oxo-4-(phenylmethyl)-3-oxazolidinyl]carbonyl]-, phenylmethyl ester, (3S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Pyridazinecarboxylic acid, tetrahydro-3-[[(4S)-2-oxo-4-(phenylmethyl)-3-oxazolidinyl]carbonyl]-, phenylmethyl ester, (3S)-(672307-41-4)
• EPA Substance Registry System: 1(2H)-Pyridazinecarboxylic acid, tetrahydro-3-[[(4S)-2-oxo-4-(phenylmethyl)-3-oxazolidinyl]carbonyl]-, phenylmethyl ester, (3S)-(672307-41-4)

Safety Data

• Hazardous Substances Data: 672307-41-4(Hazardous Substances Data)

Upstream product

• 156699-38-6 (4S)-3-<(3S)-N,N'-bis(t-butoxycarbonyl)hexahydropyridazine-3-carboxy>-4-phenylmethyl-2-oxazolidinone 
• 156699-37-5 (S)-4-benzyl-3-(5-bromopentanoyl)oxazolidine-2-one 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 4509-90-4 5-bromovaleroyl chloride 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 672307-46-9 (S)-2-((R)-2-tert-Butoxycarbonylmethyl-5-methyl-hexanoyl)-3-((S)-1-isopropyl-2-oxo-butylcarbamoyl)-tetrahydro-pyridazine-1-carboxylic acid benzyl ester 
• 672307-47-0 (S)-2-((R)-2-Carboxymethyl-5-methyl-hexanoyl)-3-((S)-1-isopropyl-2-oxo-butylcarbamoyl)-tetrahydro-pyridazine-1-carboxylic acid benzyl ester 
• 672307-45-8 1-(phenylmethyl) hydrogen (3S)-2-[(2R)-2-[2-(1,1-dimethylethoxy)-2-oxoethyl]-5-methyl-1-oxohexyl]hexahydro-1,3-pyridazinedicarboxylate 
• 65632-62-4 (3S)-hexahydro-1,3-pridazinedicarboxylic acid 1-(phenylmethyl) ester 

Relevant articles and documents

Stereochemical Definition and Chirospecific Synthesis of the Peptide Deformylase Inhibitor Sch 382583

The recently reported natural product Sch 382583 (1), an inhibitor of peptide deformylase, has been synthesized in 16 steps from commercially available starting materials. The three chiral centers were set by a combination of chiral auxiliary and chiral p