2584-64-7

Basic information

• Product Name: Glycine, N-(phenylthioxomethyl)-
• CAS NO: 2584-64-7
• Molecular Formula: C9H9NO2S
• Molecular Weight: 195.242
• Mol File: 2584-64-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Glycine, N-(phenylthioxomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(phenylthioxomethyl)-(2584-64-7)
• EPA Substance Registry System: Glycine, N-(phenylthioxomethyl)-(2584-64-7)

Safety Data

• Hazardous Substances Data: 2584-64-7(Hazardous Substances Data)

Upstream product

• 56-40-6 glycine 
• 942-91-6 Carboxymethyl dithiobenzoate 
• 93-58-3 benzoic acid methyl ester 
• 1499-53-2 ethyl hippurate 
• 7471-86-5 methyl benzimidate 
• 5873-86-9 methyl thiobenzoate 
• 87386-07-0 N-(thiobenzoyl)glycine ethyl ester 

Downstream Products

• 495-69-2 Hippuric Acid 
• 98-91-9 thiobenzoic acid 
• 13895-59-5 4-(2,6-dimethyl-pyran-4-ylidene)-2-phenyl-4H-thiazol-5-one 
• 24053-33-6 5-acetylsulfanyl-2-phenyl-thiazole 
• 138190-35-9 (Z)-4-(4-methoxybenzylidene)-2-phenylthiazol-5(4H)-one 
• 16446-30-3 4-benzylidene-2-phenyl-4H-thiazol-5-one 
• 70489-49-5 4-[2-(5,7-dimethoxy-4-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-ethylidene]-2-phenyl-4H-thiazol-5-one 
• 16446-03-0 4-[2-(5'-chloro-8'-methoxy-3',4'-dihydro-2'H-spiro[[1,3]dioxolane-2,1'-naphthalen]-3'-yl)-ethylidene]-2-phenyl-4H-thiazol-5-one 
• 13895-44-8 4-(1-benzyl-2,6-dimethyl-1H-pyridin-4-ylidene)-2-phenyl-4H-thiazol-5-one 
• 35317-64-7 4-(2-acetoxy-1-acetoxymethyl-ethylidene)-2-phenyl-4H-thiazol-5-one 
• 35317-65-8 4-((Z)-2-acetoxy-1-methyl-ethylidene)-2-phenyl-4H-thiazol-5-one 
• 35317-69-2 diphenylacetic acid 4-(2-acetoxy-1-acetoxymethyl-vinyl)-2-phenyl-thiazol-5-yl ester 
• 35317-70-5 1,3-diacetoxy-2-(5-acetoxy-2-phenyl-thiazol-4-yl)-propene 
• 32607-18-4 4-(2-acetoxy-1-acetoxymethyl-ethyl)-2-phenyl-4H-thiazol-5-one 

Relevant articles and documents

-

-

A total synthesis and structural aspects of racemic 8-oxygenated tetracyclines

A stereoselective total synthesis of the first 8-oxygenated tetracycline derivatives 43 and 4 is described. Key steps for the construction of the tetracycline skeleton are the condensation of the tetralone aldehyde 24 with the thiazolone 32 followed by co