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13-ethyl-3-methoxy-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-ol (non-preferred name) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5914-86-3

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5914-86-3 Usage

Family

Cyclopentaphenanthrene

Structure

Contains a cyclopentane ring fused to a phenanthrene ring

Steroidal derivative

Yes

Ethyl group

Present at the 13th position

Methoxy group

Present at the 3rd position

Saturated compound

Yes, indicated by multiple hydrogen atoms in the decalin ring system

Potential applications

Pharmacological and medicinal chemistry (further research needed)

Research status

Further research required to fully understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 5914-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5914-86:
(6*5)+(5*9)+(4*1)+(3*4)+(2*8)+(1*6)=113
113 % 10 = 3
So 5914-86-3 is a valid CAS Registry Number.

5914-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9S,13S,14S,17S)-13-Ethyl-3-methoxy-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-ol

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

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

More Details:5914-86-3 SDS

5914-86-3Relevant academic research and scientific papers

Synthesis of 13-alkyl-gon-4-ones

-

, (2008/06/13)

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

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