3619-20-3

Basic information

• Product Name: Glycine, N-[(4-methylphenyl)sulfonyl]-, hydrazide
• Synonyms: N-(toluene-4-sulfonyl)-glycine hydrazide;p-Tosylglycin-hydrazid;N-(4-toluenesulfonyl)-glycinyl hydrazide;N-Hydrazinocarbonylmethyl-4-methyl-benzenesulfonamide;N-(Toluol-4-sulfonyl)-glycin-hydrazid;N--glycinhydrazid;Tosyl-glycinhydrazid;
• CAS NO: 3619-20-3
• Molecular Formula: C9H13N3O3S
• Molecular Weight: 243.287
• Mol File: 3619-20-3.mol
• Article Data: 2

Chemical Properties

• Melting Point: 155 - 156 °C
• CAS DataBase Reference: Glycine, N-[(4-methylphenyl)sulfonyl]-, hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[(4-methylphenyl)sulfonyl]-, hydrazide(3619-20-3)
• EPA Substance Registry System: Glycine, N-[(4-methylphenyl)sulfonyl]-, hydrazide(3619-20-3)

Safety Data

• Hazardous Substances Data: 3619-20-3(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 2645-02-5 methyl tosylglycinate 
• 5465-67-8 ethyl N-tosylglycinate 

Downstream Products

• 110062-67-4 N-(5-thioxo-4,5-dihydro-[1,3,4]oxadiazol-2-ylmethyl)-toluene-4-sulfonamide 
• 886147-31-5 benzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 354146-82-0 2-furaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 1285705-99-8 3,4-methylenedioxybenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 444050-60-6 4-methylbenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 1285705-98-7 4-nitrobenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 331426-83-6 4-methoxybenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 443977-89-7 3-methoxy-4-hydroxybenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 328077-25-4 4-bromobenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 1285705-94-3 2-fluorobenzaldehyde N-(4-toluenesulfonyl)-glycinyl hydrazone 
• 1285705-92-1 acetophenone N-(4-toluenesulfonyl)-glycinyl hydrazone 

Relevant articles and documents

Synthesis and Antiviral Evaluation of New N-acylhydrazones Containing Glycine Residue

N-acylhydrazones containing glycine residue 3a-j and 8a-h were synthesized as HIV-1 capsid protein assembly inhibitors. The structures of the novel N-acylhydrazone derivatives were characterized using different spectroscopic methods. Antiviral activity de