51646-16-3

Basic information

• Product Name: 2-[(4-CHLOROBENZYL)SULFANYL]-5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE
• Synonyms: 2-[(4-CHLOROBENZYL)SULFANYL]-5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE;4-CHLOROBENZYL 5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-2-YL SULFIDE;2-{[(4-chlorophenyl)methyl]sulfanyl}-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine
• CAS NO: 51646-16-3
• Molecular Formula: C₁₄H₁₃ClN₄S
• Molecular Weight: 304.8
• Mol File: 51646-16-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(4-CHLOROBENZYL)SULFANYL]-5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-CHLOROBENZYL)SULFANYL]-5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE(51646-16-3)
• EPA Substance Registry System: 2-[(4-CHLOROBENZYL)SULFANYL]-5,7-DIMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE(51646-16-3)

Safety Data

• Hazardous Substances Data: 51646-16-3(Hazardous Substances Data)

Upstream product

• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 815-68-9 3-acetylpentane-2,4-dione 
• 41266-78-8 3-<(p-chlorobenzyl)thio>-5-amino-1,2,4-triazole 
• 123-54-6 acetylacetone 

Relevant articles and documents

On triazoles. XXXV. The reaction of 5-amino-1,2,4-triazoles with di- and triketones

The reaction of 5-amino-3-Q-1H-1,2,4-triazoles 1 with aliphatic, aromatic and cyclic 1,3-diketones, 1,4-diketones, and different linear and non linear triketones was studied. It was proved that in case of unsymmetrical aliphatic 1,3-diketones the regiochemical outcome of the reaction was influenced by steric factors. In case of triacetylmethane and 3-(4-chlorobenzyl)-2,4-pontanedione the splitting of one acetyl group from the reactant was observed during the reaction. A liner triketone, namely the 2,4,6-trioxoheptane reacted as a simple 1,3-diketone.

2-(Alkylthio)-1,2,4-triazolo[1,5-a]pyrimidines as adenosine cyclic 3',5'-monophosphate phosphodiesterase inhibitors with potential as new cardiovascular agents

A series of new 2-(alkylthio)-5,7-disubstituted-1,2,4-triazolo[1,5-a]pyrimidines have been prepared as inhibitors of cAMP phosphodiesterase from various tissues. These derivatives were prepared via ring closure of various requisite 3-amino-1,2,4-triazole

2-SUBSTITUTED-S-TRIAZOLO[1,5A]-PYRIMIDINES

2-Substituted-s-triazolo[1,5a]pyrimidines are disclosed which are useful as inhibitors of phosphodiesterase enzymes or intermediates in the production process. Such comoounds are of the following structure: wherein X, R, R1, R2 and R3 are as defined herei