62155-27-5 Usage
General Description
ACETIC ACID AMINOOXO METHYL ESTER, also known as methyl acetoacetate, is a chemical compound commonly used as a solvent, in the production of pharmaceuticals and as a starting material for the synthesis of other chemicals. It is a colorless, flammable liquid with a fruity odor, and is soluble in water and common organic solvents. It is a versatile compound that is used as a precursor in the production of many important chemicals, including agrochemicals, dyes, and fragrance ingredients. It is also used in the synthesis of flavorings and perfumes, and as a chemical intermediate in the manufacture of pharmaceuticals. Additionally, it is used in the production of polymers and plastics. Due to its versatility and wide range of applications, ACETIC ACID AMINOOXO METHYL ESTER is an important and widely used chemical compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 62155-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,5 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62155-27:
(7*6)+(6*2)+(5*1)+(4*5)+(3*5)+(2*2)+(1*7)=105
105 % 10 = 5
So 62155-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H5NO3/c1-7-3(6)2(4)5/h1H3,(H2,4,5)
62155-27-5Relevant articles and documents
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Gabbai,A.,Posternak,T.
, p. 1531 - 1543 (1971)
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Copper-Catalysed (Diacetoxyiodo)benzene-Promoted Aerobic Esterification Reaction: Synthesis of Oxamates from Acetoacetamides
Zhang, Zhiguo,Gao, Xiaolong,Yu, Haifeng,Zhang, Guisheng,Liu, Jianming
supporting information, p. 3406 - 3411 (2018/07/31)
A copper-catalysed (diacetoxyiodo)benzene-promoted aerobic esterification reaction of acetoacetamides was developed for the synthesis of oxamates, which are useful precursors in synthetic organic chemistry. This practical and mild synthetic approach proceeded at 25 °C under open-air conditions and afforded methyl 2-oxo-2-(phenylamino)acetates in good to excellent yields combined with C?C σ-bond cleavage and formal oxidative C?H bond functionalization. A mechanism is proposed. (Figure presented.).
DECOMPOSITION PRODUCTS OF HALONITROACETIC ACID DERIVATIVES
Yurtanov, A. I.
, p. 120 - 122 (2007/10/02)
The halonitro group O2NCHX of chloro- and bromonitroacetic acid derivatives underwent reduction to H2NCO upon boiling.The same derivatives decomposed to oxalic acid upon long storage.Likely chemical transformation pathways are discussed. Keywords: chloro- and bromonitroacetic acids, reduction, oxalic acid, amides.
