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2-Hexenedioic acid, (E)-, also known as (E)-2-Hexenedioic acid or trans-2-Hexenedioic acid, is an organic compound with the chemical formula C6H8O4. It is a conjugated dienoic acid, meaning it contains two carbon-carbon double bonds separated by a single carbon atom. The (E)- configuration indicates that the double bonds are in a trans arrangement, with the hydroxyl groups (-OH) on opposite sides of the molecule. 2-Hexenedioic acid, (E)- is a key intermediate in the synthesis of various chemicals and can be used in the production of polymers, pharmaceuticals, and other industrial products. It is also known for its role in the metabolism of certain compounds in living organisms.

2583-24-6

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2583-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2583-24-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2583-24:
(6*2)+(5*5)+(4*8)+(3*3)+(2*2)+(1*4)=86
86 % 10 = 6
So 2583-24-6 is a valid CAS Registry Number.

2583-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-2-enedioic acid

1.2 Other means of identification

Product number -
Other names 2-Hexenedioic acid

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:2583-24-6 SDS

2583-24-6Upstream product

2583-24-6Relevant academic research and scientific papers

Electrochemical hydrogenation of bioprivileged: Cis, cis -muconic acid to trans -3-hexenedioic acid: From lab synthesis to bench-scale production and beyond

Bateni, Hamed,Dell'Anna, Marco Nazareno,Laureano, Mathew,Matthiesen, John E.,Paskach, Thomas J.,Tessonnier, Jean-Philippe,Zaza, Ludovic,Zembrzuski, Michael P.

, p. 6456 - 6468 (2021/09/10)

The integration of microbial and electrochemical conversions in hybrid processes broadens the portfolio of products accessible from biomass. For instance, sugars and lignin monomers can be biologically converted to cis,cis-muconic acid (ccMA), a bioprivileged intermediate, and further electrochemically upgraded to trans-3-hexenedioic acid (t3HDA). This novel monounsaturated monomer is gaining increasing attention as it can substitute adipic acid in Nylon 6,6 to introduce desired properties and yield polyamides with performance advantages. The implementation of t3HDA for advanced polymer production is, however, hampered by the low productivities achieved to date, in the order of milligrams per hour per cm2. Here, we report on new synergies between microbial and electrochemical conversions and present a simple strategy to enhance the productivity of t3HDA by over 50 times. Specifically, we show that the broth composition has a dramatic role on the subsequent electrochemical step. Broth with neutral pH and high ccMA titer obtained from bacteria was found to enhance the electrochemical hydrogenation while impeding the parasitic hydrogen evolution reaction. As a result, high productivities were achieved under industrially-relevant current densities (200-400 mA cm-2). The effect of other parameters that are key for scale up and continuous operation, namely reactor configuration, potentiostatic/galvanostatic operation mode, and cathode material are also discussed. The experimental results served as input parameters for a detailed technoeconomic analysis and the blueprint of a hybrid microbial electrosynthesis process for t3HDA production.

A biocompatible alkene hydrogenation merges organic synthesis with microbial metabolism

Sirasani, Gopal,Tong, Liuchuan,Balskus, Emily P.

supporting information, p. 7785 - 7788 (2014/08/05)

Organic chemists and metabolic engineers use orthogonal technologies to construct essential small molecules such as pharmaceuticals and commodity chemicals. While chemists have leveraged the unique capabilities of biological catalysts for small-molecule production, metabolic engineers have not likewise integrated reactions from organic synthesis with the metabolism of living organisms. Reported herein is a method for alkene hydrogenation which utilizes a palladium catalyst and hydrogen gas generated directly by a living microorganism. This biocompatible transformation, which requires both catalyst and microbe, and can be used on a preparative scale, represents a new strategy for chemical synthesis that combines organic chemistry and metabolic engineering. Reduction to practice: A hydrogenation reaction has been developed that employs hydrogen generated in situ by a microorganism and a biocompatible palladium catalyst to reduce alkenes on a synthetically useful scale. This type of transformation, which directly combines tools from organic chemistry with the metabolism of a living organism for small-molecule production, represents a new strategy for chemical synthesis.

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