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21-O-Acetyl 6β-Hydroxy Dexamethasone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72559-77-4

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72559-77-4 Usage

Chemical Properties

Off-White Solid

Uses

Protected metabolite of Dexamethasone (D298800).

Check Digit Verification of cas no

The CAS Registry Mumber 72559-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,5 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72559-77:
(7*7)+(6*2)+(5*5)+(4*5)+(3*9)+(2*7)+(1*7)=154
154 % 10 = 4
So 72559-77-4 is a valid CAS Registry Number.

72559-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(6R,8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-6,11,17-trihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

1.2 Other means of identification

Product number -
Other names 21-O-Acetyl 6|A-Hydroxy Dexamethasone

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:72559-77-4 SDS

72559-77-4Relevant academic research and scientific papers

Selenium dioxide oxidation of steroidal 1,4-dien-3-ones. A simple and convenient route to 6-hydroxycorticosteroids

Terasawa,Okada

, p. 307 - 317 (2007/10/02)

A convenient one-step procedure for the chemical synthesis of 6-hydroxycorticosteroids involving allylic oxidation of selenium dioxide is described.

Synthesis and topical antiinflammatory potencies of a series of 6-keto- and Δ6-6-acyloxybetamethasone derivatives

Draper,Berkenkopf,Carlon,Fernandez,Monahan,Lutsky

, p. 317 - 322 (2007/10/02)

6-Keto and Δ6-6-acyloxybetamethasone esters were synthesized, and tested for topical antiinflammatory potency using a modification of the Tonelli croton ear assay. The introduction of a 6-keto group generally led to retention of topical antiinflammatory potencies when compared to the corresponding 6-desoxycorticoids. In contrast, introduction of the Δ6-6-acyloxy moiety into betamethasone 17,21-dipropionate reduced antiinflammatory potency.

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