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63518-06-9

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  • [(16E)-10,13-dimethyl-17-oxo-16-(pyrrolidin-1-ylmethylidene)-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

    Cas No: 63518-06-9

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  • [(16E)-10,13-dimethyl-17-oxo-16-(pyrrolidin-1-ylmethylidene)-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate cas 63518-06-9

    Cas No: 63518-06-9

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  • Hangzhou Fandachem Co.,Ltd
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  • [(16E)-10,13-dimethyl-17-oxo-16-(pyrrolidin-1-ylmethylidene)-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

    Cas No: 63518-06-9

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63518-06-9 Usage

Description

(16E)-17-oxo-16-(pyrrolidin-1-ylmethylidene)androst-5-en-3-yl acetate is a complex chemical compound belonging to the class of androstane steroids. It is a derivative of androst-5-en-3-yl acetate, featuring a pyrrolidin-1-ylmethylidene group at the 16th carbon atom and a keto group at the 17th carbon atom. (16E)-17-oxo-16-(pyrrolidin-1-ylmethylidene)androst-5-en-3-yl acetate is commonly utilized in pharmaceutical research and drug development due to its potential biological activities and applications in medicine and biochemistry.

Uses

Used in Pharmaceutical Research and Drug Development:
(16E)-17-oxo-16-(pyrrolidin-1-ylmethylidene)androst-5-en-3-yl acetate is used as a research compound for exploring its potential biological activities and applications in the development of new pharmaceuticals. Its unique structure and properties make it a promising candidate for further investigation in the fields of medicine and biochemistry.
Used in Medicine:
As a member of the androstane steroid class, (16E)-17-oxo-16-(pyrrolidin-1-ylmethylidene)androst-5-en-3-yl acetate may have therapeutic applications in medicine. Its specific effects and uses will depend on its mode of action and further research is required to fully understand its potential in this area.
Used in Biochemistry:
(16E)-17-oxo-16-(pyrrolidin-1-ylmethylidene)androst-5-en-3-yl acetate may also find use in biochemical research, where it can be employed to study the interactions and mechanisms of androstane steroids. This could lead to a better understanding of their roles in biological systems and the development of targeted therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 63518-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63518-06:
(7*6)+(6*3)+(5*5)+(4*1)+(3*8)+(2*0)+(1*6)=119
119 % 10 = 9
So 63518-06-9 is a valid CAS Registry Number.

63518-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(16E)-10,13-dimethyl-17-oxo-16-(pyrrolidin-1-ylmethylidene)-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:63518-06-9 SDS

63518-06-9Downstream Products

63518-06-9Relevant articles and documents

D-Ring modification of steroids: synthesis of isoxazole annulated steroids from des D-formyl alkyne via 1,3-dipolar cycloaddition reaction

Nongthombam, Geetmani Singh,Boruah, Romesh Chandra

, p. 2853 - 2861 (2021)

The reaction of 17,17-dichloro-androst-16(E)-chloromethylene with secondary amine base afforded substitution products of exocyclic D-ring ketones, in contrast to the reaction of alkaline base which cleaved steroidal D-ring to des-D formyl alkyne. The des-

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