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Benzyl(3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-(triisopropylsilanyloxy)piperidine-1-carboxylate is a complex chemical compound featuring a piperidine ring with hydroxy, benzyl, and carboxylate ester groups, as well as triisopropylsilane moieties. This piperidine carboxylate derivative is characterized by its specific stereochemistry and functional groups, making it a versatile building block in organic chemistry synthesis for applications across the pharmaceutical, agrochemical, and materials industries.

873945-27-8

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873945-27-8 Usage

Uses

Used in Pharmaceutical Industry:
Benzyl(3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-(triisopropylsilanyloxy)piperidine-1-carboxylate is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to be modified and incorporated into various drug molecules. Its unique stereochemistry and functional groups allow for the creation of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Benzyl(3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-(triisopropylsilanyloxy)piperidine-1-carboxylate is used as a precursor in the development of novel agrochemicals, such as pesticides and herbicides. Its structural features enable the design of molecules with targeted biological activity and improved environmental compatibility.
Used in Materials Industry:
Benzyl(3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-(triisopropylsilanyloxy)piperidine-1-carboxylate is utilized as a component in the synthesis of advanced materials, including polymers and coatings. Its functional groups and stereochemistry contribute to the development of materials with specific properties, such as improved durability, adhesion, or biocompatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 873945-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,9,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 873945-27:
(8*8)+(7*7)+(6*3)+(5*9)+(4*4)+(3*5)+(2*2)+(1*7)=218
218 % 10 = 8
So 873945-27-8 is a valid CAS Registry Number.

873945-27-8SDS

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 benzyl (3R,4R,5S)-3-hydroxy-4-(4-hydroxyphenyl)-5-tri(propan-2-yl)silyloxypiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (3R,4R,5S)-3-hydroxy-4-(4-hydroxy-phenyl)-5-triisopropylsilanyl-oxy-piperidine-1-carboxylic acid benzyl ester

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:873945-27-8 SDS

873945-27-8Relevant academic research and scientific papers

Substituted piperidines as therapeutic compounds

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, (2009/02/10)

Described are compounds of the general formula (I) and pharmaceutically acceptable salt thereof, in which R2, R3, W,and X have the definitions illustrated in detail in the description, as beta-secretase, cathepsin D, plasmepsin II an

Substituted Piperidines as Renin Inhibitors

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Page/Page column 50-51, (2009/12/24)

Compounds of the general formula (I) in which the meanings of the substituents R1, R2, R3, R4, X, Z and n as stated in claim 1 have renin-inhibiting properties and can be used as medicines.

Substituted piperidines as therapeutic compounds

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Page/Page column 31, (2008/12/08)

Use of compounds of the general formula (1) and pharmaceutically acceptable salt thereof, in which R1, R2, R3, R4, W, X, Z and n have the definitions illustrated in detail in the description, as beta-secretase, cathepsin D, plasmepsin II and/or HIV protease inhibitors.

Organic compounds

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Page/Page column 29, (2010/11/30)

The present invention relates to substituted piperidines of the general formula (I), where R1, R2, R3, R4, R5, Q and X have the definitions elucidated in more detail in the description, to a process for their preparation and to the use of these compounds as medicines, in particular as renin inhibitors. Moreover, the enzymatic substrate portion of the compound is simultaneously a substrate for a membrane transporter.

SUBSTITUTED 4-PHENYLPIPERIDINES

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Page/Page column 49, (2008/06/13)

The application relates to substituted 4-phenylpiperidines of the general formula and their salts, preferably their pharmaceutically acceptable salts, in which R2, R3, W and X have the meanings explained in the description, a process for their preparation and the use of these compounds as medicines, especially as renin inhibitors.

3,4,5-SUBSTITUTED PIPERIDINES AS RENIN INHIBITORS

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Page/Page column 46, (2008/06/13)

The application relates to novel substituted piperidines of the general formula (II) in which R1, R2', R2'', R4', X, Z, m and n have the meanings defined in the description, to a process for the preparation thereof and to the use of these compounds as medicines, especially as renin inhibitors.

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