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3,4-dihydroxy-5-(3-methylbut-2-enyl)-2-(2-methyl-1-oxobutyl)-4-(4-methyl-1-oxopent-3-enyl)cyclopent-2-en-1-one is a complex organic compound characterized by a cyclopentenone core structure. It features multiple functional groups, such as hydroxyl, enone, and alkyl moieties, along with unsaturated side chains of varying lengths and substitutions. This intricate molecular architecture endows the compound with unique properties that may be harnessed in various scientific and industrial applications.

25422-83-7

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25422-83-7 Usage

Uses

Used in Medicinal Chemistry:
3,4-dihydroxy-5-(3-methylbut-2-enyl)-2-(2-methyl-1-oxobutyl)-4-(4-methyl-1-oxopent-3-enyl)cyclopent-2-en-1-one is used as a key intermediate in the synthesis of pharmaceutical compounds due to its diverse functional groups and unique structural features. These characteristics facilitate the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 3,4-dihydroxy-5-(3-methylbut-2-enyl)-2-(2-methyl-1-oxobutyl)-4-(4-methyl-1-oxopent-3-enyl)cyclopent-2-en-1-one serves as a versatile building block for creating a wide range of organic molecules. Its reactivity and the presence of multiple functional groups make it suitable for various synthetic pathways, leading to the formation of complex organic structures.
Used in Materials Science:
3,4-dihydroxy-5-(3-methylbut-2-enyl)-2-(2-methyl-1-oxobutyl)-4-(4-methyl-1-oxopent-3-enyl)cyclopent-2-en-1-one is utilized in materials science for the development of novel materials with specific properties. Its unique molecular structure and functional groups can contribute to the creation of materials with tailored characteristics for use in various applications, such as coatings, adhesives, or advanced composites.
Used in Research and Development:
This complex compound is also used in research and development settings to study the reactivity and biological activity of complex organic molecules. Its unique structural features provide a platform for investigating the interactions between molecules and their potential applications in various fields, including drug discovery and materials innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 25422-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,2 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25422-83:
(7*2)+(6*5)+(5*4)+(4*2)+(3*2)+(2*8)+(1*3)=97
97 % 10 = 7
So 25422-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O5/c1-7-14(6)18(23)17-19(24)15(10-8-12(2)3)21(26,20(17)25)16(22)11-9-13(4)5/h8-9,14-15,25-26H,7,10-11H2,1-6H3

25422-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydroxy-2-(2-methylbutanoyl)-5-(3-methylbut-2-enyl)-4-(4-methylpent-3-enoyl)cyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names EINECS 246-967-4

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:25422-83-7 SDS

25422-83-7Upstream product

25422-83-7Downstream Products

25422-83-7Relevant academic research and scientific papers

A kinetic study on the isomerization of hop α-acids

Jaskula, Barbara,Kafarski, Pawel,Aerts, Guido,De Cooman, Luc

, p. 6408 - 6415 (2008)

In this article, a detailed study on hop α-acid isomerization kinetics is presented. Because of the complex wort matrix and interfering interactions occurring during real wort boiling (i.e., trub formation and α-acids/iso-α-acids complexation), this investigation on α-acid isomerization kinetics was performed in aqueous buffer solution as a function of time (0-90 min) and heating temperature (80-100°C). Rate constants and activation energies for the formation of individual isc-α-acids were determined. It was found that iso-α-acid formation follows first-order kinetics and Arrhenius behavior. Differences in activation energies for the formation of trans- and cis-isomers were noticed, the activation energy for the formation of trans-iso-α-acids being approximately 9 kJmol-1 lower.

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