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6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID is a chemical compound with the molecular formula C14H18O5. It is an organic carboxylic acid that belongs to the family of phenylacetic acids. 6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID features a six-carbon chain with a phenyl ring attached to the fourth carbon and two methoxy groups attached to the phenyl ring. Additionally, it contains a ketone group on the sixth carbon of the chain, which contributes to its unique structure and reactivity. These characteristics make it a valuable component in the synthesis of pharmaceuticals and organic compounds, with potential applications in medicinal chemistry and drug discovery.

79381-16-1

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79381-16-1 Usage

Uses

Used in Pharmaceutical Synthesis:
6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID is utilized as a starting material for the synthesis of a wide range of organic compounds. Its reactivity and functional groups make it suitable for various chemical reactions, leading to the creation of diverse molecules with potential applications in different industries.
Used in Medicinal Chemistry:
6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID plays a significant role in medicinal chemistry, where it is employed for the design and development of new therapeutic agents. Its structural features enable it to interact with biological targets, potentially leading to the discovery of novel drugs with improved efficacy and safety profiles.
Used in Drug Discovery:
6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID is also used in drug discovery processes, where it serves as a potential lead compound for further optimization and development. Its unique properties and reactivity make it a promising candidate for the identification of new pharmacological agents with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 79381-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79381-16:
(7*7)+(6*9)+(5*3)+(4*8)+(3*1)+(2*1)+(1*6)=161
161 % 10 = 1
So 79381-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O5/c1-18-10-7-8-13(19-2)11(9-10)12(15)5-3-4-6-14(16)17/h7-9H,3-6H2,1-2H3,(H,16,17)

79381-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2,5-DIMETHOXYPHENYL)-6-OXOHEXANOIC ACID

1.2 Other means of identification

Product number -
Other names 6-(2,5-Dimethoxy-phenyl)-6-oxo-hexansaeure

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:79381-16-1 SDS

79381-16-1Relevant academic research and scientific papers

A synthesis of 6-(2,5-dimethoxy-4-(2-aminopropyl)phenyl)-hexylthiol. A ligand for conjugation with fluorescent cadmium selenide/zinc sulfide core/shell nanocrystals and biological imaging

Tomlinson, Ian D.,Grey, Jesse L.,Rosenthal, Sandra J.

, p. 777 - 790 (2007/10/03)

The synthesis of 6-(2,5-dimethoxy-4-(2-aminopropyl)phenyl)hexylthiol, an (agonist with a very high affinity for the 5HT)2A serotonin receptor subtype is reported. This agonist was designed to be attached to highly fluorescent cadmium selenide/zinc sulfide core/shells via a thiol at the end of a linker arm. This conjugate has applications in biological assays and biological imaging.

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