2273-41-8 Usage
Uses
Used in Organic Synthesis:
α,α-Dimethyl-1-piperidineacetonitrile 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.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, α,α-Dimethyl-1-piperidineacetonitrile serves as a key component in the development of new drugs. Its ability to be modified and incorporated into complex molecular structures makes it valuable for the creation of novel therapeutic agents.
Used in Agrochemical Industry:
α,α-Dimethyl-1-piperidineacetonitrile is also utilized in the agrochemical sector for the synthesis of pesticides and other crop protection agents. Its role in these applications is to contribute to the development of more effective and targeted products.
Used in Specialty Chemicals:
α,α-Dimethyl-1-piperidineacetonitrile finds application in the production of specialty chemicals, where its unique properties can be harnessed to create high-value products for specific industries, such as the fragrance, flavor, or dye industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2273-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2273-41:
(6*2)+(5*2)+(4*7)+(3*3)+(2*4)+(1*1)=68
68 % 10 = 8
So 2273-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2/c1-9(2,8-10)11-6-4-3-5-7-11/h3-7H2,1-2H3
2273-41-8Relevant academic research and scientific papers
Popov, Yu. V.,Mokhov,Tankabekyan
, p. 1135 - 1138 (2013)
Reactions of 2-adamantan-2-one, acetone cyanohydrin, and amine lead to the formation of substituted 2-amino-2-cyanoadamantanes. The reaction is of a general character as has been proved by examples on a series of ketones and amines and it proceeds through
Transamination of a-amino nitriles
Popov,Mokhov,Tankabekyan
, p. 21 - 24 (2014/03/21)
α-Amino nitriles containing a primary amino group undergo transamination with aliphatic and aromatic amines under mild conditions with high yields. A probable reaction mechanism involving intermediate elimination of cyanide ion has been proposed.
COMPOUNDS HAVING ACTIVITY AT THE GLYCINE TRANSPORTER GLYT1 AND USES THEREOF
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Page/Page column 13, (2009/09/25)
The present invention relates to compounds of formula (I), salts or solvates thereof, their use in the manufacture of medicaments for treating neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder. Th
Novel and convenient aldolization of methyl 3,3,3-trifluoropyruvate using enamines instead of ketones
Palecek, Jiri,Paleta, Oldrich
, p. 521 - 524 (2007/10/03)
Piperidine enamines derived from acetone, acetophenone, cyclopentanone and cyclohexanone react easily in minutes with methyl 3,3,3-trifluoropyruvate (1) to afford products of the aldol condensation in high yields at room temperature, which is in contrast to the direct aldolization of 1 with the ketones.
