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1229-33-0

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1229-33-0 Usage

General Description

(16beta)-3-methoxyestra-1,3,5(10)-trien-16-ol, also known as 16beta-methoxyestradiol, is a synthetic derivative of estradiol, a naturally occurring hormone in the human body. It has been studied for its potential therapeutic effects, particularly in the treatment of cancer and other diseases. 16beta-methoxyestradiol has been shown to have anti-angiogenic and anti-cancer properties, making it a promising candidate for the development of new drugs for cancer treatment. Research also suggests that it may have neuroprotective and anti-inflammatory effects, making it a potentially valuable compound for the treatment of neurological and inflammatory conditions. Overall, 16beta-methoxyestradiol is a compound with diverse potential therapeutic applications, and continued research into its properties and mechanisms of action is warranted.

Check Digit Verification of cas no

The CAS Registry Mumber 1229-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1229-33:
(6*1)+(5*2)+(4*2)+(3*9)+(2*3)+(1*3)=60
60 % 10 = 0
So 1229-33-0 is a valid CAS Registry Number.

1229-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxyestra-1,3,5(10)-trien-16β-ol

1.2 Other means of identification

Product number -
Other names 16.β.-Estradiol-3-methyl ether

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:1229-33-0 SDS

1229-33-0Relevant articles and documents

Mass spectrometry of ring D hydroxylated 3-methoxy-1,3,5(10)-estratrienes

Schade,Ihn,Vokoun,Schoenecker,Schubert

, p. 547 - 561 (1980)

Mass spectra and fragmentation patterns of the epimeric 17-,16-,15- and 14-hydroxy derivatives of 3-methoxy- 1,3,5(10)-estratriene are compared. The main fragmentation pathways are differently influenced, depending on the position of the hydroxy group. The different configuration of the hydroxy groups is reflected only in the spectra of the epimeric 15- and 14-hydroxy compounds. Possibilities of mass spectrometric differentiation between the hydroxy-estratrienes are discussed.

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