154410-82-9 Usage
Description
(Z)-Methyl 2-(hydroxyimino)-2-(pyridin-2-yl)acetate is a chemical compound belonging to the pyridine and carboxylic acid ester chemical classes, characterized by its molecular formula C9H9N2O3. This light yellow solid is commonly utilized in organic synthesis and pharmaceutical research, and is recognized for its antimicrobial and insecticidal properties.
Uses
Used in Pharmaceutical Research:
(Z)-Methyl 2-(hydroxyimino)-2-(pyridin-2-yl)acetate is used as a key intermediate in the production of various drugs and fine chemicals, playing a crucial role in the development of new pharmaceutical compounds.
Used in Agriculture:
(Z)-Methyl 2-(hydroxyimino)-2-(pyridin-2-yl)acetate is used as an antimicrobial and insecticidal agent for potential applications in agriculture, helping to protect crops and enhance yield.
Used in Organic Synthesis:
(Z)-Methyl 2-(hydroxyimino)-2-(pyridin-2-yl)acetate is used as a reagent in organic synthesis, contributing to the creation of a wide range of chemical products.
Used in Material Science:
(Z)-Methyl 2-(hydroxyimino)-2-(pyridin-2-yl)acetate may have potential applications in the development of new materials and biological molecules, expanding its utility beyond traditional fields.
Check Digit Verification of cas no
The CAS Registry Mumber 154410-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,1 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 154410-82:
(8*1)+(7*5)+(6*4)+(5*4)+(4*1)+(3*0)+(2*8)+(1*2)=109
109 % 10 = 9
So 154410-82-9 is a valid CAS Registry Number.
154410-82-9Relevant articles and documents
Total Synthesis of the Natural Herbicide MBH-001 and Analogues
Barber, David M.,D?ller, Uwe,Dietrich, Hansj?rg,Hoffmann, Michael G.,Kocakaya, Tamer,Kuhn, Birgit,Maier, Martin E.,Morkunas, Marius,Schmutzler, Dirk,Schnatterer, Stefan
, p. 2271 - 2290 (2020/04/23)
The first total synthesis of the natural herbicide MBH-001 (1) is reported. Structurally it is a 2-methyloxazol-5(2H)-one with a (1-hydroxyethyl) substituent at the 2-position. By relying on cyclic nitrones, a flexible route to MBH-001 and relevant analogues was developed. Key steps include the reaction of a 2-hydroxyimino ester with an aldehyde to form a 5-oxo-2,5-dihydrooxazole 3-oxide. In an aldol-type reaction, the anion of these cyclic nitrones reacted with an aldehyde at the 2-position. A final reduction of the nitrone to the corresponding imine using zinc led to the target compounds. The cyclic nitrones are also accessible by reacting an α-keto acid with an oxime. These two versatile synthetic routes enabled us to prepare the first MBH-001 analogues for structure activity relationship analysis of the herbicidal efficacy. Thus, furthering our aim of developing new herbicides to tackle the ever-growing problem of weed resistance.
DERIVATIVES OF 6,7-DIHYDRO-5H-IMIDAZO[1,2-α]IMIDAZOLE-3- CARBOXYLIC ACID AMIDES
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Page/Page column 131, (2009/07/03)
Derivatives of 6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-carboxylic acid amide exhibit good inhibitory effect upon the interaction of CAMs and Leukointegrins and are thus useful in the treatment of inflammatory disease.
