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7-(DIETHYLAMINO)-5-METHYL-S-TRIAZOLO[1,5-A]PYRIMIDINE CAS NO.15421-84-8
- Min.Order: 1 Metric Ton
- Payment Terms: T/T
- Available Specifications:
- Product Details
Keywords
- s-Triazolo[1,5-a]pyrimidine,7-(diethylamino)-5-methyl- (6CI,8CI)
- 4-(Diethylamino)-6-methyl-1,3,3a,7-tetraazaindene
- 5-Methyl-7-(diethylamino)-1,2,4-triazolo[1,5-a]pyrimidine
Quick Details
- ProName: 7-(DIETHYLAMINO)-5-METHYL-S-TRIAZOLO[1...
- CasNo: 15421-84-8
- Molecular Formula: C10H15N5
- Appearance: powder
- Application: Vasodilator;PDGF antagonist
- DeliveryTime: in stock
- PackAge: according to the customers
- Port: shanghai
- ProductionCapacity: 1 Metric Ton/
- Purity: 99%
- Storage: Inert atmosphere,Room Temperature
- Transportation: by sea sea and couier
- LimitNum: 1 Metric Ton
- Related Substances: 1
- Residue on Ignition: 1
- Heavy Metal: 1
- Valid Period: 1
- 1: 2
- 1: 2
Superiority
8.4 g of 5-methyl-7-chloro-s-triazolo-(1,5-a)-pyrimidine were suspended in 30 cc of water and 7.3 g of diethylamine added. After 2 hours heating with stirring, the mixture was concentrated under vacuum. The residue was recrystallized from n-heptane. This process yielded 8.1 g of the 5-methyl-7- diethylamino-s-triazolo-(1,5-a)-pyrimidine having a melting point of 103°C to 104°C. The hydrochloride produced in the usual manner had a melting point of 212°C.Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes. An experimental teratogen. Other experimental reproductive effects. A coronary vasodilator. When heated to decomposition it emits toxic fumes of NOx. See also MINES.
Details
8.4 g of 5-methyl-7-chloro-s-triazolo-(1,5-a)-pyrimidine were suspended in 30 cc of water and 7.3 g of diethylamine added. After 2 hours heating with stirring, the mixture was concentrated under vacuum. The residue was recrystallized from n-heptane. This process yielded 8.1 g of the 5-methyl-7- diethylamino-s-triazolo-(1,5-a)-pyrimidine having a melting point of 103°C to 104°C. The hydrochloride produced in the usual manner had a melting point of 212°C.Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes. An experimental teratogen. Other experimental reproductive effects. A coronary vasodilator. When heated to decomposition it emits toxic fumes of NOx. See also MINES.