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3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) is a complex organic compound with a steroid-like structure. It is a derivative of cyclopenta[a]phenanthrene and contains a propanoic acid group. This molecule is highly stereochemically complex due to its multiple chiral centers and methyl groups.

41020-65-9

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41020-65-9 Usage

Uses

Used in Pharmaceutical Industry:
3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) is used as a pharmaceutical agent for its potential therapeutic properties. The complex structure and multiple chiral centers of 3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) may contribute to its unique interactions with biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) is used as a research tool in the field of organic chemistry. Its stereochemical complexity provides opportunities for studying the effects of chirality on chemical reactions and the development of novel synthetic routes to access such complex molecules.
Used in Material Science:
3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) is used in the development of new materials with unique properties. The steroid-like structure and functional groups present in 3-[(7R,8S,9S,10R,13R,14S)-7-(methoxycarbonyl)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name) may offer potential applications in the creation of advanced materials for various industries, such as nanotechnology or polymer science.

Check Digit Verification of cas no

The CAS Registry Mumber 41020-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41020-65:
(7*4)+(6*1)+(5*0)+(4*2)+(3*0)+(2*6)+(1*5)=59
59 % 10 = 9
So 41020-65-9 is a valid CAS Registry Number.

41020-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Mexrenone

1.2 Other means of identification

Product number -
Other names mexrenone

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:41020-65-9 SDS

41020-65-9Relevant academic research and scientific papers

Processes for preparation of 3-keto-7alpha-alkoxycarbonyl-delta-4,5- steroids and intermediates useful therein

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Page 60, (2008/06/13)

Multiple novel reaction schemes, novel process steps and novel intermediates are provided for the synthesis of epoxymexrenone and other compounds of Formula I wherein:-A-A- represents the group -CHR4-CHR5- or -CR4=CR5- R3, R4 and R5 are independently selected from the group consisting of hydrogen, halo, hydroxy, lower alkyl, lower alkoxy, hydroxyalkyl, alkoxyalkyl, hydroxycarbonyl, cyano, varyloxy;R1 represents an alpha-oriented lower alkoxycarbonyl or hydroxyalkyl radical;-B-B- represents the group -CHR6-CHR7- or an alpha- or beta- oriented group: where R6 and R7 are independently selected from the group consisting of hydrogen, halo, lower alkoxy, acyl, hydroxyalkyl, alkoxyalkyl, hydroxycarbonyl, alkyl, alkoxycarbonyl, acyloxyalkyl, cyano and aryloxy; andR8 and R9 are independently selected from the group consisting of hydrogen, hydroxy, halo, lower alkoxy, acyl, hydroxyalkyl, alkoxyalkyl, hydroxycarbonyl, alkyl, alkoxycarbonyl, acyloxyalkyl, cyano and aryloxy, or R8 and R9 together comprise a carbocyclic or heterocyclic ring structure, or R8 or R9 together with R6 or R7 comprise a carbocyclic or heterocyclic ring structure fused to the pentacyclic D ring.

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