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17-Iodoandrosta-5,16-dien-3β-ol, 99%|1552017|32138-69-5

17-Iodoandrosta-5,16-dien-3β-ol, 99%

Cat. No JK1552017_25_G
J&K Chemical

Product Information

Product Name
17-Iodoandrosta-5,16-dien-3β-ol, 99%
Brand Name
J&K
Product Number
1552017
CAS
32138-69-5
Molecular Formula
C19H27IO
Molecular Weight
398.33
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
(3S,8R,9S,10R,13S,14S)-17-Iodo-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopentaaphenanthren-3-ol
PubChem CID
11069352
IUPAC Name
(3S,8R,9S,10R,13S,14S)-17-iodo-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopentaaphenanthren-3-ol
InChI Key
DHZJEYGWSNDRGN-USOAJAOKSA-N
SMILES
CC@12CCC@@H(CC1=CCC@@H3C@@H2CCC@4(C@H3CC=C4I)C)O

Properties

Melting Point
173.4 - 174.2

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
H336
Precautionary Statement
P264
P270
P330
P280
P261
P271
P405
P319
P301+P317
P302+P352
P332+P317
P305+P351+P338
P264+P265
P337+P317
P304+P340
P403+P233
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Four-Step Synthesis of Abiraterone Acetate from Dehydroepiandrosterone
Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2016-09
DOI: 10.1007/s11094-016-1459-1

A versatile synthesis of 17-heteroaryl androstenes via palladium-mediated Suzuki cross-coupling with heteroaryl boronic acids
Publication Name: Steroids
Publication Date: 2006-07
DOI: 10.1016/j.steroids.2006.02.004

Novel C-17-Heteroaryl Steroidal CYP17 Inhibitors/Antiandrogens: Synthesis, in Vitro Biological Activity, Pharmacokinetics, and Antitumor Activity in the LAPC4 Human Prostate Cancer Xenograft Model
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2005-03-25
DOI: 10.1021/jm040202w

17-Iodoandrosta-5,16-dien-3β-ol, 99%

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