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986-96-9

986-96-9

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  • [(8R,9S,10R,13S,14S,17R)-17-acetyl-3-acetyloxy-6,10,13-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate

    Cas No: 986-96-9

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  • [(8R,9S,10R,13S,14S,17R)-17-acetyl-3-acetyloxy-6,10,13-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate cas 986-96-9

    Cas No: 986-96-9

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986-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 986-96-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 986-96:
(5*9)+(4*8)+(3*6)+(2*9)+(1*6)=119
119 % 10 = 9
So 986-96-9 is a valid CAS Registry Number.

986-96-9SDS

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 [(8R,9S,10R,13S,14S,17R)-17-acetyl-17-acetyloxy-6,10,13-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[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

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

More Details:986-96-9 SDS

986-96-9Downstream Products

986-96-9Relevant articles and documents

Preparation method of palace progesterone

-

, (2021/11/03)

The invention relates to the technical field of preparation of pharmaceutical active pharmaceutical chemicals, in particular to a preparation method of palace progesterone. To the preparation method, 17 α - hydroxyl progesterone is used as a substrate, and nucleophilic addition reaction is carried out in sequence. An epoxidation reaction, an open-loop addition reaction, an elimination reaction, an esterification reaction and a hydrolysis reaction are adopted to obtain the toecliptin progesterone, and a precious metal catalyst and a carcinogenic solvent are not used in the preparation process simultaneously. ≥ 91%.

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