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75262-69-0

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75262-69-0 Usage

Chemical Properties

White Solid

Uses

An impurity of Dexamethasone (D298800), Desoxymethasone,

Check Digit Verification of cas no

The CAS Registry Mumber 75262-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75262-69:
(7*7)+(6*5)+(5*2)+(4*6)+(3*2)+(2*6)+(1*9)=140
140 % 10 = 0
So 75262-69-0 is a valid CAS Registry Number.

75262-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-7,8,11,12,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthrene-17-carboxylic acid

1.2 Other means of identification

Product number -
Other names 17|A-Carboxy 17-Desoxymethasone

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:75262-69-0 SDS

75262-69-0Upstream product

75262-69-0Downstream Products

75262-69-0Relevant articles and documents

9α-fluoro-16α-methyl-3,11-dioxoan-drosta-1,4-diene-17β- carboxylic acid: Catemeric hydrogen bonding and acetic acid solvation in a steroidal keto acid related to dexamethasone

Lalancette, Roger A.,Thompson, Hugh W.

, p. o274-o276 (2003)

The title keto acid crystallizes as a solvate, C21H25-FO4·C2H4 O2, with two molecules each of steroid and acetic acid per asymmetric unit. The former are approximately parallel, with opposite end-to-end orientation, and form translational carboxyl-to-ketone hydrogen-bonding catemers [O...;O = 2.679 (6) and 2.650 (5) A, and O-H...O = 165 and 162] that involve the 3-ketone group and follow the a axis. The acetic acid molecules are paired by hydrogen bonding, and neither they nor the F atom nor the 11-ketone group play any overt role in the hydrogen-bonding scheme of the steroid. Intermolecular C-H...O=C close contacts involving three different neighboring molecules exist to the 11-ketone group, the steroidal carboxyl group and one of the acetic acid molecules.

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