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2304-17-8

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2304-17-8 Usage

Description

(8S,9S,10S,13S,14S,17S)-2,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12, 14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one is a steroid compound with a cyclopenta[a]phenanthren structure, characterized by a molecular formula of C21H32O3 and a molecular weight of 332.48 g/mol. It features two hydroxy groups, three methyl groups, and a ketone group at position 3, with its stereochemistry defined by the specific arrangement of these functional groups on the steroid framework. This chemical is likely to exhibit biological activities associated with steroids, and its potential applications would depend on its specific properties and interactions with biological systems.

Uses

Used in Pharmaceutical Industry:
(8S,9S,10S,13S,14S,17S)-2,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12, 14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one is used as a pharmaceutical compound for its potential biological activities. Given its steroidal nature, it may be involved in the development of drugs targeting various medical conditions, such as hormonal imbalances, inflammation, or other steroid-responsive diseases.
Used in Research and Development:
In the field of research and development, (8S,9S,10S,13S,14S,17S)-2,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12, 14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one serves as a valuable chemical entity for studying the effects of steroidal compounds on biological systems. Its unique structure and functional groups make it an interesting subject for exploring new mechanisms of action and potential therapeutic applications.
Used in Chemical Synthesis:
(8S,9S,10S,13S,14S,17S)-2,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12, 14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one can be utilized as a starting material or intermediate in the synthesis of more complex steroidal compounds. Its specific stereochemistry and functional groups may be exploited to create novel molecules with tailored properties for various applications, including pharmaceuticals, agrochemicals, or other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 2304-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2304-17:
(6*2)+(5*3)+(4*0)+(3*4)+(2*1)+(1*7)=48
48 % 10 = 8
So 2304-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O3/c1-18-11-17(22)16(21)10-12(18)4-5-13-14(18)6-8-19(2)15(13)7-9-20(19,3)23/h10-11,13-15,22-23H,4-9H2,1-3H3/t13-,14+,15+,18+,19+,20+/m1/s1

2304-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (8R,9S,10S,13S,14S,17S)-2,17-dihydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names 2,17beta-Dihydroxy-17-methylandrosta-1,4-dien-3-one

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:2304-17-8 SDS

2304-17-8Upstream product

2304-17-8Downstream Products

2304-17-8Relevant articles and documents

A facile two-step high yield approach to 2-oxasteroids

Frimer,Hameiri-Buch,Ripshtos,Gilinsky-Sharon

, p. 5693 - 5706 (2007/10/02)

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