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5-bromo-3,6-dihydroxyandrostan-17-one-3-acetate is a synthetic steroidal compound characterized by the presence of a bromine atom at the 5th carbon position, two hydroxyl groups at the 3rd and 6th carbon positions, and an acetate group at the 17th carbon position. This molecule is derived from the androstane skeleton, which is a common structure in many natural and synthetic steroids. The acetate group at the 17th position indicates that it is an esterified form of the steroid, which can influence its solubility and metabolic properties. 5-bromo-3,6-dihydroxyandrostan-17-one-3-acetate may be of interest in pharmaceutical or chemical research due to its unique structure and potential biological activities, although specific applications or effects would depend on the context of its use.

4229-69-0

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4229-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4229-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4229-69:
(6*4)+(5*2)+(4*2)+(3*9)+(2*6)+(1*9)=90
90 % 10 = 0
So 4229-69-0 is a valid CAS Registry Number.

4229-69-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-acetoxy-5-bromo-6β-hydroxy-5α-androstan-17-one

1.2 Other means of identification

Product number -
Other names 5α-bromo-3β,6β-dihydroxyandrostan-17-one 3-acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4229-69-0 SDS

4229-69-0Upstream product

4229-69-0Relevant academic research and scientific papers

Synthetic study of strongylophorines: stereoselective construction of the characteristic lactone bridge

Oikawa, Yuya,Uchiyama, Daiki,Shirasawa, Takuya,Oikawa, Masato,Ishikawa, Yuichi

supporting information, p. 3949 - 3951 (2016/08/09)

Herein, we report an efficient construction of the lactone bridge of strongylophorine-2, which is a meroditerpenoid isolated from Strongylophora durissima and an inhibitor for HIF-1 transcriptional pathway. Starting from dehydroepiandrosterone acetate, the characteristic lactone has been constructed in 5.4% over 18 steps by employing, (1) modified oxy radical-mediated C–H functionalization at the C24 methyl group, and (2) four-step manipulation of C4 quaternary carbon stereogenic center. The lactone synthesized here is expected as a precursor for (8-desmethyl)strongylophorine-2 which is of particular interest in terms of structure–activity relationships in the inhibition of HIF-1 transcriptional pathway.

COMPOUNDS AND METHODS FOR TREATING NEOPLASIA

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Page/Page column 93-94, (2012/02/13)

The invention features compounds, pharmaceutical compositions and methods useful for the treatment of neoplasia. In particular embodiments, the compounds of the invention are useful for the treatment of multidrug resistant neoplasia.

19-Oxygenated-5α-androstanes for the enhancement of libido

-

, (2008/06/13)

Derivatives of 19-oxygenated-5α-androstanes are described which are useful in enhancing the libido and related psychic attitudes in mammals.

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