17a-Hydroxy-11-deoxycorticosterone-21-acetate

CAS : 640-87-9

Ref. TR-H934800

Informations sur le produit

• Nom: 17a-Hydroxy-11-deoxycorticosterone-21-acetate
• Synonymes: Pregn-4-ene-3,20-dione, 21-(acetyloxy)-17-hydroxy-, Corticosterone, 11-deoxy-17-hydroxy-, 21-acetate (6CI), Pregn-4-ene-3,20-dione, 17,21-dihydroxy-, 21-acetate (8CI), 21-(Acetyloxy)-17-hydroxypregn-4-ene-3,20-dione, 11-Deoxycortisol 21-acetate, 17,21-Dihydroxypregn-4-ene-3,20-dione 21-acetate, 17-Hydroxy-21-acetoxyprogesterone, 21-Acetoxy-17-hydroxypregn-4-ene-3,20-dione, 21-Acetoxy-17α-hydroxyprogesterone, 4-Pregnene-17α,21-diol-3,20-dione 21-acetate, Cortexolone 21-acetate, Cortodoxon 21-acetate, NSC 81196, Reichstein substance S 21-acetate, Reichstein-S-acetate, Reichstein's substance S 21-acetate
• Marque: TRC
• Description: Impurity Hydrocortisone EP Impurity KApplications 17α-Hydroxy-11-deoxycorticosterone-21-acetate (Hydrocortisone EP Impurity K) is an acetate substance 'S' - a synthetic steroid as carbaryl synergist.References Brown-Grant, K., et al.: J. Endocrinol., 38, 145 (1967), Brzezowska, E., et al.: J. Steroid Molec. Biol., 57, 357 (1996), Kamihira, M., et al.: Agric. Biol. Chem., 51, 407 (1987), Fabre, C., et al.: Biotechnol. Bioeng., 64, 392 (1999),

Propriétés chimiques

• Masse moléculaire: 388.4972
• Formule: C₂₃H₃₂O₅
• Couleur/Forme: White
• InChI: InChI=1S/C23H32O5/c1-14(24)28-13-20(26)23(27)11-8-19-17-5-4-15-12-16(25)6-9-21(15,2)18(17)7-10-22(19,23)3/h12,17-19,27H,4-11,13H2,1-3H3/t17-,18+,19+,21+,22+,23+/m1/s1
• Code InChI: InChIKey=HPAKILCZTKWIFK-JZTHCNPZSA-N
• SMILES: CC(=O)OCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C