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   ChemNet > CAS > 302-96-5 2'H-Androst-2-eno [3,2-c] pirazol-17-ol, 17-metil-, (5a, 17b) -

302-96-5 2'H-Androst-2-eno [3,2-c] pirazol-17-ol, 17-metil-, (5a, 17b) -

ürün Ad? 2'H-Androst-2-eno [3,2-c] pirazol-17-ol, 17-metil-, (5a, 17b) -
E? anlaml? 2'H-5a-Androst-2-eno [3,2-c] pirazol-17b-ol, 17-metil- (8CI); Siklopenta [7,8] fenantro [2,3-c] pirazol-1-ol, 1,2,3,3a, 3b, 4,5,5a, 6,7,10,10a, 10b, 11,12,12a-hekzadekahidro-1,10a, 12a-trimetil- (6CI, 7CI); 17-Metil-5a-androstano[3,2-c]pirazol-17b-ol; 17-Metil-pirazolo [4 ', 3 ': 2,3] -5a-androstan-17b-ol; 17a-Metil-17b-hidroksi-5a-androstano(3,2-c)pirazol; 17b-Hidroksi-17-metil-5a-androstano[3,2-c]pirazol; 17b-Hidroksi-17a-metil-5a-androstano[3,2-c]pirazol; Anabol; Androstanazol; Androstanazol; Androstanazolestanazol; Estazol; NSC233046; Stanabolik; Stanazolol; Stanozolol; Stromba; Strombaject; Tevabolin; 14833 kazanmak; Winstroid; Winstrol; Winstrol Deposu; Winstrol V
ingilizce ad? 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-methyl-, (5a,17b)-;2'H-5a-Androst-2-eno[3,2-c]pyrazol-17b-ol, 17-methyl- (8CI); Cyclopenta[7,8]phenanthro[2,3-c]pyrazol-1-ol,1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethyl-(6CI,7CI); 17-Methyl-5a-androstano[3,2-c]pyrazol-17b-ol; 17-Methyl-pyrazolo[4',3':2,3]-5a-androstan-17b-ol; 17a-Methyl-17b-hydroxy-5a-androstano(3,2-c)pyrazole; 17b-Hydroxy-17-methyl-5a-androstano[3,2-c]pyrazole; 17b-Hydroxy-17a-methyl-5a-androstano[3,2-c]pyrazole; Anabol; Androstanazol; Androstanazole; Androstanazolestanazol; Estazol; NSC233046; Stanabolic; Stanazolol; Stanozolol; Stromba; Strombaject; Tevabolin; Win 14833; Winstroid; Winstrol; Winstrol Depot; Winstrol V
Moleküler Formülü C21H32N2O
Molekül A??rl??? 328.55
CAS kay?t numaras? 302-96-5
Moleküler Yap?s? 302-96-5 2'H-Androst-2-eno [3,2-c] pirazol-17-ol, 17-metil-, (5a, 17b) -
Yo?unluk 1.129g/cm3
Kaynama noktas? 490.8°Cat760mmHg
Alevlenme noktas? 250.7°C
Tehlike Sembolleri
Risk Kodlar?
Güvenlik A??klamas? x." target="_blank">Human systemic effects by ingestion: jaundice. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.:;
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