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(2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid, also known as 2,5-dimethyl-2,4-hexadienedioic acid, is a carboxylic acid with a chemical formula C8H10O4. It is a diene acid with two double bonds and two methyl groups on the carbon chain. (2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid is known for its versatile reactivity and ability to undergo various chemical reactions, making it a valuable starting material in the synthesis of a wide range of compounds.

20514-40-3

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20514-40-3 Usage

Uses

Used in Pharmaceutical Industry:
(2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid is used as a starting material for the synthesis of various pharmaceuticals. Its ability to undergo esterification, reduction, and oxidation reactions allows for the production of different derivatives with diverse functional groups, which can be further utilized in the development of new drugs and pharmaceutical intermediates.
Used in Agrochemical Industry:
In the agrochemical industry, (2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid serves as a key intermediate in the synthesis of various agrochemicals. Its reactivity and functional group diversity make it suitable for the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Organic Compounds Synthesis:
(2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid is used as a starting material in the synthesis of various organic compounds. Its versatile nature and reactivity enable the production of a wide range of specialty chemicals, which can be used in different industries such as plastics, coatings, and adhesives.
Used in Research Applications:
Due to its unique structure and reactivity, (2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid is also used in research applications. It can be employed as a model compound to study various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 20514-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,1 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20514-40:
(7*2)+(6*0)+(5*5)+(4*1)+(3*4)+(2*4)+(1*0)=63
63 % 10 = 3
So 20514-40-3 is a valid CAS Registry Number.

20514-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z,4Z)-2,5-dimethylhexa-2,4-dienedioic acid

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-hexa-2c,4c-diendisaeure

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:20514-40-3 SDS

20514-40-3Upstream product

20514-40-3Relevant academic research and scientific papers

Diene conformation in the naturally occurring tricarboxylic acid, telfairic acid, by Raman spectroscopy

Edwards, Howell G.M.,Edwards, Raymond L.,Hartley, Melanie J.,Quinn, Michael

, p. 24 - 29 (2007/10/03)

The conformational geometry of the two C{double bond, short}C bonds in a naturally occurring dienetricarboxylic acid, telfairic acid, isolated from Xylaria telfairii, has been determined by Raman spectroscopy. This application of analytical Raman spectroscopy is important because infrared, UV and NMR spectroscopic techniques have failed to provide sufficient information for the determination of the diene geometry. Several specially synthesised model dienecarboxylic acids with known diene conformations were used to calibrate the Raman data. The natural extract from X. telfairii was shown to be a mixture of both cis (Z) and trans (E) forms whereas the purified extract was predominantly the trans isomer. Raman data also suggest that the established method for the preparation of a trans-trans sorbic acid is open to debate. Further applications of the Raman technique for the determination of diene conformation of fungal metabolite extracts are proposed.

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