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17-hydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate, also known as hydrocortisone acetate, is a synthetic steroid hormone derivative belonging to the class of corticosteroids. It possesses anti-inflammatory, immunosuppressive, and anti-allergic properties, making it a valuable pharmaceutical ingredient in various medications.

1249-67-8

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1249-67-8 Usage

Uses

Used in Pharmaceutical Industry:
17-hydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate is used as an active pharmaceutical ingredient for the treatment of conditions such as eczema, dermatitis, and allergic reactions. It is effective in reducing inflammation and suppressing the immune response, providing relief to affected individuals.
Used in Topical Medications:
In the form of creams, ointments, and topical solutions, 17-hydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate is used as a local treatment applied directly to the affected area of the skin. This allows for targeted relief and minimizes systemic side effects associated with oral corticosteroids.

Check Digit Verification of cas no

The CAS Registry Mumber 1249-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1249-67:
(6*1)+(5*2)+(4*4)+(3*9)+(2*6)+(1*7)=78
78 % 10 = 8
So 1249-67-8 is a valid CAS Registry Number.

1249-67-8SDS

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 [2-[(8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

1.2 Other means of identification

Product number -
Other names UNII-1N587LS3RF

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:1249-67-8 SDS

1249-67-8Relevant articles and documents

A by the 3,17-dione steroid preparing steroid the synthetic method of the compound of

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Paragraph 0102; 0103; 0142-0147, (2017/03/14)

The invention discloses a synthetic method of steroid type drugs and intermediates, in particular relates to a synthetic method for preparing 17-hydroxy-20-ketone steroid compounds from 3,17-diketone steroids, and belongs to the field of synthesis of drugs. The method takes 3,17-diketone steroids as raw materials and adopts a conventional, environment-friendly, low-toxicity reagent, and the steroid type drugs such as cortisone, hydrocortisone, metacortandracin, or hydroprednisone, or intermediates 17alpha-hydroxy-20-ketone compounds are prepared simply and conveniently at high yield by selective protection of C3 or (and) C11-ketone group, Wittig reaction of C17, selective oxidization of 17(20)-position double bonds and halogenating replacement. The aftertreatment is simple, few three wastes are generated, the reaction selectivity is good, the yield is high, and byproducts anti-pregnancy steroidal drugs and steroidal compounds can be obtained. The raw materials are easy to get, the cost is low and the synthetic process is simple; the synthetic method is suitable for industrial production.

Process for the preparation of 17-haloethynyl steroids, and novel 17-haloethynyl steroids

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, (2008/06/13)

17-haloethynyl steroids of the partial formula STR1 wherein R1 is hydrogen or methyl, R2 is alkyl of 1-4 carbon atoms, acyl of 1-7 carbon atoms, trimethylsilyl, 2-tetrahydropyranyl, or nitrate, X is bromine or iodine, and V is methyl

Process and intermediates for the preparation of 17 alphahydroxyprogesterones and corticoids from an enol steroid

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, (2008/06/13)

This invention discloses an improved process for the production of corticoids from 17α-hydroxy steroids utilizing peroxymonosulfate.

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