1756-18-9 Usage
Description
alpha,beta-dihydroxyisovaleric acid, also known as 2,3-dihydroxyisovaleric acid, is a dihydroxy monocarboxylic acid derived from isovaleric acid with hydroxy groups substituted at positions 2 and 3. This organic compound has potential applications in various industries due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Industry:
alpha,beta-dihydroxyisovaleric acid is used as an intermediate compound for the synthesis of various pharmaceuticals and biologically active molecules. Its ability to form hydrogen bonds and interact with other molecules makes it a valuable building block in drug development.
Used in Chemical Synthesis:
alpha,beta-dihydroxyisovaleric acid is used as a key component in the synthesis of complex organic molecules, particularly in the fields of organic chemistry and materials science. Its unique functional groups allow for a wide range of reactions and modifications, leading to the creation of novel compounds with specific properties.
Used in Research and Development:
alpha,beta-dihydroxyisovaleric acid serves as a valuable research tool for studying the properties and reactivity of dihydroxy monocarboxylic acids. It can be used to investigate various chemical reactions, mechanisms, and the development of new synthetic methods.
Used in Analytical Chemistry:
alpha,beta-dihydroxyisovaleric acid can be employed as a reference compound or standard in analytical chemistry for the calibration of instruments and the development of new analytical techniques. Its distinct chemical properties make it suitable for various analytical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1756-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1756-18:
(6*1)+(5*7)+(4*5)+(3*6)+(2*1)+(1*8)=89
89 % 10 = 9
So 1756-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O4/c1-5(2,9)3(6)4(7)8/h3,6,9H,1-2H3,(H,7,8)
1756-18-9Relevant articles and documents
Kinetics and Mechanism of the Oxidation of Unsaturated Carboxylic Acids by Methyltributylammonium Permanganate in Methylene Chloride Solutions
Perez-Benito, Joaquin F.,Lee, Donald G.
, p. 3239 - 3243 (2007/10/02)
The product obtained when permanganate is reduced by unsaturated carboxylic acids under anhydrous conditions is manganese(III).The rate of reaction, which is subject to acid catalysis, exhibits a Hammet ρ value of 1.11 and inverse secondary isotope effects (kH/kD = 0.96-0.98) when the hydrogens on the double bond are replaced by deuterium.The involvement of a free-radical process is indicated by the formation of polymer during the oxidation of acrylic and methacrylic acids.The reaction is believed to be initiated by formation of an organometallic complex in which the double bond is a η2 ligand on manganese.Rearrangement of this complex results in the formation of a reactive manganate(V) cyclic diester, which undergoes a rapid (free-radical) reduction to manganese(III).
The stereochemistry of 1,2,3-trihydroxy-3-methylbutane and 2,3-dihydroxy-3-methylbutyric acid.
Nielsen,Larsen,Lemmich
, p. 967 - 970 (2007/10/05)
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