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(1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol is a complex organic compound that features a cyclopentanol ring with multiple functional groups. It consists of a tert-butyldiphenylsilyloxy group, a methylene group, and a trityloxyMethyl group. (1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol is chiral, as indicated by the descriptors (1R,3R,4S), which describe the configuration of the different chiral centers in the molecule. The presence of silyloxy and trityl groups suggests its potential use as a protecting group in synthetic chemistry.

1233193-58-2

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1233193-58-2 Usage

Uses

Used in Synthetic Chemistry:
(1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol is used as a protecting group for [application reason] in synthetic chemistry. The silyloxy and trityl groups in the compound provide a means to protect certain functional groups during chemical reactions, allowing for selective reactions to occur at other sites within the molecule.
Used in Pharmaceutical Industry:
(1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol is used as a key intermediate in the synthesis of complex pharmaceutical compounds. Its unique structure and functional groups make it a valuable building block for the development of new drugs, particularly in the context of medicinal chemistry.
Used in Materials Science:
(1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol is used as a component in the development of advanced materials, such as polymers and composites. (1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol's structural features may contribute to the properties of these materials, potentially leading to new applications in various industries.
Note: The specific application reasons and industries mentioned above are hypothetical and would depend on the actual research and development carried out by chemists and companies working with (1R,3R,4S)-4-(tert-butyldiphenylsilyloxy)-2-Methylene-3-(trityloxyMethyl)cyclopentanol. Further details about its use and properties would likely be proprietary to the chemist or company using it.

Check Digit Verification of cas no

The CAS Registry Mumber 1233193-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,1,9 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1233193-58:
(9*1)+(8*2)+(7*3)+(6*3)+(5*1)+(4*9)+(3*3)+(2*5)+(1*8)=132
132 % 10 = 2
So 1233193-58-2 is a valid CAS Registry Number.

1233193-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(tert-butyl-diphenyl-silanyloxy)-2-methylene-3-trityloxymethyl-cyclopentanol

1.2 Other means of identification

Product number -
Other names (1R,3R,4S)-4-(tert-Butyl-diphenyl-silanyloxy)-2-methylene-3-trityloxymethyl-cyclopentanol

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:1233193-58-2 SDS

1233193-58-2Relevant academic research and scientific papers

SYNTHETIC METHOD OF ENTECAVIR AND INTERMEDIATE COMPOUNDS THEREOF

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Page/Page column 58; 59; 65; 66, (2017/10/31)

The present invention relates to preparation method of drugs and intermediate compounds thereof, in particular, to preparation method of entecavir, intermediate compounds thereof and synthetic method of said intermediate compounds.

NOVEL INTERMEDIATE AND PROCESS FOR PREPARING ENTECAVIR USING SAME

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, (2011/10/19)

The present invention relates to a novel, high-yield and low-cost method for preparing entecavir, [1-S-(1α,3α,4β)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one, an antiviral agent, and novel intermediates used therein.

NOVEL INTERMEDIATE AND PROCESS FOR PREPARING ENTECAVIR USING SAME

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Page/Page column 17-18, (2010/07/09)

The present invention relates to a novel, high-yield and low-cost method for preparing entecavir, [1-S-(1α,3α,4,β]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one, an antiviral agent, and novel intermediates used therein.

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