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174264-48-3

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174264-48-3 Usage

Description

Methyl-1-(6-tert-butyldimethylsylyl-4’-hydroxyraloxifene)-2,3,4-tri-O-acetyl--D-glycopyranuronate is a complex organic compound that serves as an intermediate in the synthesis of the metabolite of Raloxifene. Raloxifene is a nonsteroidal estrogen receptor mixed agonist/antagonist, which means it can both activate and inhibit the effects of estrogen in the body. Methyl-1-(6-tert-butyldimethylsylyl-4’-hydroxyraloxifene)-2,3,4-tri-O-acetyl--D-glycopyranuronate is characterized by its orange foam appearance and is used in the pharmaceutical industry for the development of drugs that target estrogen receptor-related conditions.

Uses

Used in Pharmaceutical Industry:
Methyl-1-(6-tert-butyldimethylsylyl-4’-hydroxyraloxifene)-2,3,4-tri-O-acetyl--D-glycopyranuronate is used as an intermediate in the synthesis of Raloxifene metabolites for the development of pharmaceutical drugs. The application reason is its role in creating a nonsteroidal estrogen receptor mixed agonist/antagonist, which can be used to treat conditions related to estrogen receptor activity, such as osteoporosis and certain types of cancer.
Used in Synthesis of Raloxifene Metabolites:
Methyl-1-(6-tert-butyldimethylsylyl-4’-hydroxyraloxifene)-2,3,4-tri-O-acetyl--D-glycopyranuronate is used as a key component in the synthesis process of Raloxifene metabolites. The application reason is its ability to facilitate the creation of a compound with mixed agonist/antagonist properties, which can be beneficial in the treatment of various medical conditions.
Chemical Properties:
The chemical properties of Methyl-1-(6-tert-butyldimethylsylyl-4’-hydroxyraloxifene)-2,3,4-tri-O-acetyl--D-glycopyranuronate include its orange foam appearance, which may be indicative of its unique structural and functional characteristics. This property could be relevant in the identification, handling, and further processing of the compound in the context of pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 174264-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,2,6 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174264-48:
(8*1)+(7*7)+(6*4)+(5*2)+(4*6)+(3*4)+(2*4)+(1*8)=143
143 % 10 = 3
So 174264-48-3 is a valid CAS Registry Number.

174264-48-3SDS

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 methyl (2S,3S,4S,5R,6S)-3,4,5-triacetyloxy-6-[4-[6-[tert-butyl(dimethyl)silyl]oxy-3-[4-(2-piperidin-1-ylethoxy)benzoyl]-1-benzothiophen-2-yl]phenoxy]oxane-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:174264-48-3 SDS

174264-48-3Downstream Products

174264-48-3Relevant articles and documents

Synthesis and estrogen receptor binding affinities of the major human metabolites of raloxifene (LY139481)

Dodge, Jeffrey A.,Lugar, Charles W.,Cho, Stephen,Osborne, John J.,Phillips, David L.,Glasebrook, Andrew L.,Frolik, Charles A.

, p. 993 - 996 (2007/10/03)

Glucuronide conjugates 1 and 2, the major metabolites of raloxifene, have been prepared and their molecular interactions with the estrogen receptor determined.

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