99705-29-0

Usage

Uses

Used in Organic Synthesis:
Methoxypivalonitrile is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Methoxypivalonitrile's reactivity and stability make it a valuable asset in the development of new and innovative organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methoxypivalonitrile serves as a key intermediate in the synthesis of various drug molecules. Its ability to be easily modified and incorporated into complex molecular structures makes it an essential component in the development of new medications and therapies.
Used in Agrochemical Industry:
Methoxypivalonitrile is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its unique properties enable the creation of effective and targeted compounds that can protect crops from pests and diseases while minimizing environmental impact.
Used in Specialty Chemicals:
In the specialty chemicals sector, Methoxypivalonitrile is employed in the production of various high-value compounds used in industries such as coatings, adhesives, and polymers. Its versatility and compatibility with a wide range of chemical reactions make it an ideal candidate for the development of novel specialty chemicals.

Upstream product

• 78-82-0 Isobutyronitrile 
• 107-30-2 chloromethyl methyl ether 
• 19295-57-9 3-hydroxy-2,2-dimethylpropionitrile 
• 18107-18-1 diazomethyl-trimethyl-silane 

Downstream Products

• 767264-22-2 3-methoxy-2,2-dimethylpropylamine 

Relevant academic research and scientific papers

Incorporation of two molecules of carbon monoxide into N-lithioketimine leading to azetidine-2,3-diones

The reaction of N-lithioketimines 1, prepared in situ from R1CN (R1 = t-Bu, 1-adamantyl, CH3OCH2(CH3)2C) and R2Li (R2 = t-Bu, s-Bu), with CO followed by addition of MeI affords azetidine-2,3-diones 2 in 40-86% yields. The reaction involves incorporation of two molecules of CO into the N- lithioketimine.

NOVEL IMIDAZO BASED HETEROCYCLES

The present invention is directed to novel imidazopyrazine and imidazopyrimidine compounds of formula (I), wherein the variables are as defined herein. The compounds of formula (I) are useful as kinase inhibitors and as such would be useful in treating ce

1-BENZYLINDOLE-2-CARBOXAMIDE DERIVATIVES

The present invention relates to i-benzylindole-2-carboxamide derivatives of formula I, or a pharmaceutically acceptable salt or solvate thereof. The invention also relates to pharmaceutical compositions comprising said 1-benzylindole-2-carboxamide deriva

Simultaneous preparation of nitriles and acrylamide or methacrylamide

Nitriles of the general formula I where R1 is a saturated or unsaturated, straight-chain, branched or cyclic alkyl radical, an aralkyl radical or an aryl radical, each of which is of not more than 20 carbon atoms and can be unsubstituted or further substituted, and (meth)acrylamide are prepared simultaneously by a process in which an aldoxime of the general formula III where R1 has the above meanings, is heated at from 50° to 180° C. in the presence of a copper(II) carboxylate and of (meth)acrylonitrile.