7779-72-8 Usage
Uses
Used in Flavor and Fragrance Industry:
ISOAMYL PYRUVATE is used as a flavoring agent for its fruity and wine-like aroma, adding unique scents and tastes to various food and beverage products.
Used in Pharmaceutical Industry:
ISOAMYL PYRUVATE is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Chemical Synthesis:
ISOAMYL PYRUVATE is used as a versatile building block in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products.
Preparation
By air oxidation of boiling isoamyl lactate; also by reacting methyl magnesium iodide over isoamyl α-hydroxy isobutyrate
Check Digit Verification of cas no
The CAS Registry Mumber 7779-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7779-72:
(6*7)+(5*7)+(4*7)+(3*9)+(2*7)+(1*2)=148
148 % 10 = 8
So 7779-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-6(2)4-5-11-8(10)7(3)9/h6H,4-5H2,1-3H3
7779-72-8Relevant academic research and scientific papers
Facile Synthesis of α-Ketocarbonyl Compounds from α-Hydroxycarbonyl Compounds
Chang, Hae Sung,Woo, Jae Chun,Lee, Kyoung Mo,Ko, Young Kwan,Moon, Surk-Sik,Kim, Dae-Whang
, p. 31 - 36 (2007/10/03)
Various α-ketocarbonyl compounds were obtained in excellent yields under mild condition from the reaction of the corresponding α-hydroxycarbonyl compounds with sodium hypobromite in the presence of HCl catalyst.
Oxidations of Dihydroxyalkanoates to Vicinal Tricarbonyl Compounds with a 4-BzoTEMPO-Sodium Bromite System or by Indirect Electrolysis Using 4-BzoTEMPO and Bromide Ion
Inokuchi, Tsutomu,Liu, Ping,Torii, Sigeru
, p. 1411 - 1414 (2007/10/02)
An efficient access to vicinal dioxoalkanoates, one of structural elements of potent competitive inhibitors of hydrolytic enzyme, from 2,3-dihydroxyalkanoates has been developed, which features an one-step procedure with a mild oxidizing system using recyclable 2, 2, 6, 6-tetramethylpiperidine-1-oxyl in combination with NaBrO2*3H2O or electrogenerated active bromine species as a real oxidant.
