7596-39-6 Usage
Uses
Used in Pharmaceutical Synthesis:
(Z)-2-propan-2-ylbut-2-enedioic acid is used as an intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its unique structure allows for the creation of a wide range of compounds with different therapeutic properties.
Used as a Corrosion Inhibitor:
In the industrial sector, (Z)-2-propan-2-ylbut-2-enedioic acid serves as an effective corrosion inhibitor. Its ability to form protective layers on metal surfaces helps prevent corrosion, making it a valuable component in the formulation of corrosion-resistant coatings and treatments.
Used as a Food Additive:
(Z)-2-propan-2-ylbut-2-enedioic acid is also utilized in the food industry as an additive. Its properties contribute to enhancing the taste, texture, and shelf life of various food products, ensuring better quality and consumer satisfaction.
Used in Organic Synthesis:
As a building block for the synthesis of various organic compounds, (Z)-2-propan-2-ylbut-2-enedioic acid plays a crucial role in the development of new chemicals with potential applications in different industries, including agriculture, materials science, and environmental management.
Check Digit Verification of cas no
The CAS Registry Mumber 7596-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7596-39:
(6*7)+(5*5)+(4*9)+(3*6)+(2*3)+(1*9)=136
136 % 10 = 6
So 7596-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O4/c1-4(2)5(7(10)11)3-6(8)9/h3-4H,1-2H3,(H,8,9)(H,10,11)/b5-3-
7596-39-6Relevant academic research and scientific papers
Asymmetric synthesis of 2-substituted butane-1,4-diols by hydrogenation of homochiral fumaramide derivatives
Jawaid, Samaila,Farrugia, Louis J.,Robins, David J.
, p. 3979 - 3988 (2007/10/03)
Diastereoselective hydrogenation of homochiral fumaramides 1 derived from (2R)-Oppolzer's sultam was observed by analysis of the 1H NMR spectra of the succinamide mixtures with de's of 77-88%. Reduction of these succinamides using LiAlH4 gave the corresponding (2S)-butane-1,4- diols and established that addition of hydrogen takes place selectively on the re-face of fumaramides 1. The stereoselectivity was confirmed by estimating the ee's from the 19F NMR spectra of the Mosher's diesters of the diols. This methodology was applied to the synthesis of selected pyrrolidine natural products in homochiral form.
Preparation of (S)-2-Substituted Succinates by Stereospecific Reductions of Fumarate and Derivatives with Resting Cells of Clostridium formicoaceticum
Eck, Richard,Simon, Helmut
, p. 13631 - 13640 (2007/10/02)
Fumarate derivatives have been reduced to (S)-2-methylsuccinate 2a, (S)-2-ethylsuccinate 3a and (S)-2-chlorosuccinate 4a in up to 1 M concentrations with Clostridium formicoaceticum.Formate was the electron donor and viologens or anthraquinone-2,6-disulphonate acted as artificial electron mediators.Reductions with freeze-dried cells in 2H2O-buffers led to the (2R,3S)--dideuterated succinate derivatives.The productivity numbers ranged from 450 to 5000 and the enantiomeric excess of all (S)-2-substituted succinates was >/= 99percent.
