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2863-88-9

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2863-88-9 Usage

Description

3-Ethoxyestra-3,5-dien-17-one is an organic compound that belongs to the class of steroids. It is characterized by its unique molecular structure, which features a steroidal framework with specific functional groups that make it a versatile compound for various applications in the pharmaceutical and chemical industries.

Uses

Used in Pharmaceutical Industry:
3-Ethoxyestra-3,5-dien-17-one is used as an intermediate in the synthesis of various steroidal compounds for pharmaceutical applications. Its structural features allow it to be a key reactant in the production of new compounds with potential therapeutic properties.
Used in Steroid Research:
In the field of steroidal studies, 3-Ethoxyestra-3,5-dien-17-one serves as a reactant in the synthesis of novel steroidal compounds with enhanced progestin activity. For instance, it was utilized in the creation of 17α-acetoxy-6,21-dimethyl-3,20-dioxo-19-norpregna-4,6-diene, a new compound that may have significant implications in hormone-related therapies and treatments.
By following the format provided for Gallotannin, the description and uses of 3-ethoxyestra-3,5-dien-17-one are organized to highlight its chemical properties and its applications in different industries, particularly in the pharmaceutical sector for steroidal research and the development of new compounds with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2863-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2863-88:
(6*2)+(5*8)+(4*6)+(3*3)+(2*8)+(1*8)=109
109 % 10 = 9
So 2863-88-9 is a valid CAS Registry Number.

2863-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxy-3,5-estradien-17-one

1.2 Other means of identification

Product number -
Other names 3-Aethoxy-oestra-3,5-dien-17-on

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:2863-88-9 SDS

2863-88-9Relevant articles and documents

Preparation method of norethindrone acetate (by machine translation)

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Paragraph 0008; 0034-0035, (2020/11/23)

The invention discloses a preparation method of norethindrone acetate and belongs to the technical field of drug preparation and processing. The method uses 19 - demethyl -4 - androstenedione as a starting raw material, protects, acetylenically, hydrolyses and esterifies 4 steps to prepare the norethindrone acetate. To the preparation method of the norethindrone acetate, the defects of a traditional process are overcome, reaction conditions are mild, impurities are reduced, overall conversion rate is high, operation is simple and convenient, and the method is suitable for industrial production and has a wide market prospect. (by machine translation)

PROCESS FOR ALKYNYLATING 16-SUBSTITUTED-17-KETO STEROIDS

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Page/Page column 20, (2013/07/05)

The invention relates to a process for ethynylating 16-methylene-17-keto steroids to the corresponding 16-methylene-17α-ethynyl-17β-hydroxy steroids by treatment with silyl-protected lithium acetylides followed by further desilylation. The resulting products are useful intermediates in the preparation of several pharmaceutically active agents, such as e.g. Nestorone? or melengestrol acetate.

Sulfuric acid adsorbed on silica gel. A multipurpose acid catalyst

Chavez,Suarez,Diaz

, p. 2325 - 2339 (2007/10/02)

A series of acid catalyzed reactions like the dehydration of alcohols, conversion of ketones to 1,3-dioxolanes and their hydrolysis, α, β- unsaturated ketones to enol ethers, and alcohols to methyl-methoxyethyl ethers are performed efficiently in high yield with sulfuric acid adsorbed on silica gel as catalyst.

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