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5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)is a complex organic chemical compound that is a methyl ester derivative of 5-heptenoic acid. It features a cyclopenten-1-yl group with a triethylsilyl-ether side chain and a carboxylic acid functional group. 5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)is characterized by a Z configuration at the double bond, which may influence its reactivity and properties in various chemical contexts. This unique structure suggests potential applications in organic synthesis, pharmaceutical development, or as a reagent in specific chemical reactions, depending on its synthesis and purification methods.

102494-28-0

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102494-28-0 Usage

Uses

Used in Organic Synthesis:
5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure, including the triethylsilyl-ether side chain and the carboxylic acid functional group, allows for versatile reactions and the formation of a wide range of organic compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)may serve as a precursor or intermediate in the synthesis of new drug candidates. Its specific functional groups and structural features could be exploited to design molecules with targeted biological activities, potentially leading to the development of novel therapeutic agents.
Used as a Reagent in Chemical Reactions:
5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)can be utilized as a reagent in specific chemical reactions, such as cross-coupling or esterification processes. Its carboxylic acid group and the presence of the triethylsilyl-ether side chain may facilitate selective reactions, making it a valuable tool in the synthesis of certain types of compounds.
While the specific applications of 5-Heptenoic acid,7-[5-oxo-3-[(triethylsilyl)oxy]-1-cyclopenten-1-yl]-,Methyl ester,(5Z)are not exhaustively detailed in the provided materials, its chemical structure and properties suggest a range of potential uses in various industries, particularly where the synthesis of novel compounds or the development of new pharmaceuticals is required. Further research and experimentation would be necessary to fully explore and validate its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 102494-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102494-28:
(8*1)+(7*0)+(6*2)+(5*4)+(4*9)+(3*4)+(2*2)+(1*8)=100
100 % 10 = 0
So 102494-28-0 is a valid CAS Registry Number.

102494-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 7-(5-oxo-3-triethylsilyloxycyclopenten-1-yl)hept-5-enoate

1.2 Other means of identification

Product number -
Other names (Z)-Methyl 7-(5-oxo-3-((triethylsilyl)oxy)cyclopent-1-en-1-yl)hept-5-enoate

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:102494-28-0 SDS

102494-28-0Relevant academic research and scientific papers

Synthesis and Gastric Antisecretory Properties of α Chain Diene Derivatives of Misoprostol

Collins, Paul W.,Gasiecki, Alan F.,Jones, Peter H.,Bauer, Raymond F.,Gullikson, Gary W.,et al.

, p. 1195 - 1201 (2007/10/02)

The synthesis and gastric antisecretory activity in dogs of seven α chain diene derivatives of misoprostol are described.The key intermediates in the preparation of these compounds were C-9 tert-butyldimethylsilyl enol ethers that were obtained by in situ

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