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547-81-9

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547-81-9 Usage

Chemical Properties

Crystalline Solid

Uses

16-Epiestriol is a metabolite of Estradiol.

Definition

ChEBI: A 3-hydroxy steroid that is 17beta-estradiol substituted by a beta-hydroxy group at position 16.

Biochem/physiol Actions

16-Epiestriol is found naturally in various animals, plants, and fungal yeast. It potentially inhibits the growth of colistins and carbapenem-resistant A. baumannii

Check Digit Verification of cas no

The CAS Registry Mumber 547-81-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 547-81:
(5*5)+(4*4)+(3*7)+(2*8)+(1*1)=79
79 % 10 = 9
So 547-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16+,17+,18+/m1/s1

547-81-9SDS

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 16β-hydroxyestradiol

1.2 Other means of identification

Product number -
Other names 16beta-hydroxyestradiol

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:547-81-9 SDS

547-81-9Relevant articles and documents

Selective Isomerization via Transient Thermodynamic Control: Dynamic Epimerization of trans to cis Diols

Macmillan, David W. C.,Oswood, Christian J.

supporting information, p. 93 - 98 (2022/01/03)

Traditional approaches to stereoselective synthesis require high levels of enantio- and diastereocontrol in every step that forms a new stereocenter. Here, we report an alternative approach, in which the stereochemistry of organic substrates is selectivel

Syntheses of 15α hydroxyestrone and 15α hydroxyestradiol

Hosoda,Yamashita,Nambara

, p. 3141 - 3145 (2007/10/12)

-

STUDIES ON THE METABOLISM OF STEROID HORMONES IN VERTEBRATES. II.

OZON,BREUER

, p. 282 - 285 (2007/10/13)

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