1421320-02-6

Basic information

• Product Name: 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide
• Synonyms: 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide
• CAS NO: 1421320-02-6
• Molecular Weight: 305.36
• Mol File: 1421320-02-6.mol

Chemical Properties

• CAS DataBase Reference: 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide(1421320-02-6)
• EPA Substance Registry System: 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide(1421320-02-6)

Safety Data

• Hazardous Substances Data: 1421320-02-6(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 593283-24-0 6-methyl-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carbohydrazide 
• 123237-03-6 ethyl 6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one-5-carboxylate 
• 100-52-7 benzaldehyde 
• 79-19-6 thiosemicarbazide 

Downstream Products

• 1421320-03-7 3,4-dihydro-5-(5-mercapto-4H-1,2,4-triazol-3-yl)-6-methyl-4-phenylpyrimidin-2(1H)-one 
• 1345840-65-4 5-(5-amino-1,3, 4-thiadiazole-2-yl)-3,4-dihydro-6-methyl-4-phenylpyrimidin-2(1H)-one 
• 1032630-79-7 5-(5-amino-1,3,4-oxadiazol-2-yl)-6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one 

Relevant articles and documents

Synthesis and comparing the antibacterial activities of pyrimidine derivatives

A series of 10 derivatives of 5-(5-amino-1,3,4-thiadiazole-2-yl)-3,4-dihydro-6-methyl-4-phenyl-pyrimidin-2(1H)-one and 10 derivatives of 3,4-dihydro-5-(5-mercapto-4H-1,2,4-triazol-3-yl)-6-methyl-4-phenyl pyrimidin-2(1H)-one have been synthesized. Among th

Novel approach for synthesis of potent antimicrobial hybrid molecules containing pyrimidine-based imidazole scaffolds

This report describes the novel approach for the synthesis and exploration of hybrid molecules containing pyrimidine-based imidazole scaffolds as potent antimicrobial agents. The targeted compounds N-(4-arylidene-2-mercapto-5-oxo-4,5-dihydro-1H -imidazol-

An efficient synthesis, characterization and anti-bacterial activity of pyrimidine bearing 1,3,4-thiadiazole derivatives

A series of pyrimidine bearing 1,3,4-thiadiazole derivatives have been synthesized and evaluated for antibacterial activity. All the structures of the newly synthesized compounds have been supported by IR, 1H and 13C NMR, GC-MS and C

Synthesis of novel Schiff bases and evaluation of their antimicrobial activities

An easy route for the synthesis of Schiff bases containing dihydropyrimidinone moiety has been reported for the first time. The dihydropyrimidinones on treatment with thiosemicarbazide result in the formation of the corresponding hydrazinecarbothioamide.

Novel synthesis and characterization of some pyrimidine derivatives of oxadiazoles, triazole and 1,3,4-thiadiazoles

In the present investigation, synthetic methods of 4-aryl-6-methyl-2-oxo-1, 2,3,4-tetrahydro pyrimidine-(5)-1,3,4-thiadiazole-2-amine (3) and 4-aryl-6-methyl-2-oxo-1,2,3,4-tetrahydro pyrimidine-(5)-1,3,4-oxadiazole-2-amine (3a) and 4-aryl-6-methyl-2-oxo-1