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5444-22-4

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5444-22-4 Usage

Description

1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL, also known as 17beta-estradiol with an additional 11beta-hydroxy substituent, is a 4-hydroxy steroid derived from the estratriene family. It possesses a unique chemical structure that allows for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL is used as a pharmaceutical compound for its potential therapeutic effects. The expression is: 1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL is used as a pharmaceutical compound for its potential therapeutic effects.
Used in Research and Development:
In the field of research and development, 1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL serves as a valuable chemical entity for studying the properties and mechanisms of steroidal compounds. The expression is: 1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL is used as a research compound for studying the properties and mechanisms of steroidal compounds.
Used in Chemical Synthesis:
1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL can be utilized as a key intermediate in the synthesis of various steroidal drugs and hormones. The expression is: 1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL is used as a synthetic intermediate for the production of steroidal drugs and hormones.
Used in Analytical Chemistry:
1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL can also be employed in analytical chemistry for the development of new methods and techniques for the detection and quantification of steroidal compounds. The expression is: 1,3,5(10)-ESTRATRIEN-3,11-BETA, 17-BETA-TRIOL is used as a reference compound for the development of analytical methods in the detection and quantification of steroidal compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 5444-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5444-22:
(6*5)+(5*4)+(4*4)+(3*4)+(2*2)+(1*2)=84
84 % 10 = 4
So 5444-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O3/c1-18-9-15(20)17-12-5-3-11(19)8-10(12)2-4-13(17)14(18)6-7-16(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15-,16-,17+,18-/m0/s1

5444-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 11β-hydroxy-17β-estradiol

1.2 Other means of identification

Product number -
Other names (8S,9S,11S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,11,17-triol

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:5444-22-4 SDS

5444-22-4Downstream Products

5444-22-4Relevant articles and documents

Compound for targeted ubiquitination degradation of ERalpha protein and application thereof

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Paragraph 0091-0093, (2020/12/30)

The invention provides a compound with estrogen receptor alpha (ERalpha) activity, and particularly provides a 1,3,5-triazine compound with a general formula (I) or a general formula (II) or a pharmaceutically acceptable salt thereof. The definitions of the groups are as described in the specification. The compound disclosed by the invention has ERalpha degradation activity and can be used for preparing medicines for treating human breast cancer and endometrial cancer.

Steroid structure and function. VII. Remarkable estrogenicity of 3-hydroxy-9β-estra-1,3,5(10)-triene-11,17-dione

Segaloff,Gabbard,Flores,Borne,Baker,Duax,Strog,Rohrer

, p. 335 - 349 (2007/10/02)

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