3010-04-6 Usage
Description
(N-BUTYLAMINO)ACETONITRILE, also known as butylaminoacetonitrile, is an organic compound that is characterized by its clear yellow to brownish liquid appearance. It is primarily used in the preparation of amides, carbamates, and sulfonamides due to its chemical properties.
Used in Pharmaceutical Industry:
(N-BUTYLAMINO)ACETONITRILE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds, including amides, carbamates, and sulfonamides. Its ability to form these compounds makes it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
(N-BUTYLAMINO)ACETONITRILE is used as a building block for the production of agrochemicals, such as pesticides and herbicides. Its versatility in forming different chemical structures allows it to be a key component in the development of effective and targeted agrochemical products.
Used in Chemical Research:
(N-BUTYLAMINO)ACETONITRILE is used as a research compound in various chemical studies and experiments. Its unique properties and reactivity make it an interesting subject for scientists to explore and understand its potential applications and reactions in different chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3010-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3010-04:
(6*3)+(5*0)+(4*1)+(3*0)+(2*0)+(1*4)=26
26 % 10 = 6
So 3010-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2/c1-2-3-5-8-6-4-7/h8H,2-3,5-6H2,1H3/p+1
3010-04-6Relevant articles and documents
Aminomethylation of lithiated nicotinamide: access to new pyridolactams
Prieur, Emilie,Azzouz, Rabah,Deguest, Geoffrey,Fruit, Corinne,Bischoff, Laurent,Marsais, Francis
, p. 437 - 440 (2008/09/17)
New 2,3-dihydropyrrolopyridinones were conveniently prepared by trapping lithiated pyridine carboxamides with highly reactive formimines. In this Letter, we report that a wide range of N-functionalised compounds can be synthesised in one step by this process, allowing the presence of ethers, acetals or ester moieties.
ELECTROCHEMICAL REDUCTIVE AMINATION. II. AMINATION OF ALIPHATIC ALDEHYDES WITH PRIMARY AMINES
Smirnov, Yu. D.,Pavlichenko, V. F.,Tomilov, A. P.
, p. 374 - 380 (2007/10/02)
The formation of a secondary amine by the electrolysis of an aqueous solution containing an aldehyde and a primary amine was studied.The formation of the secondary amines passes through the intermediate stage of an aldimine.The highest yield of secondary amine is attained at a molar ratio of primary amine to aldehyde of 1.2:1.As electrode material lead, cadmium, zinc, and copper may be used.As supporting electrolyte a phosphate buffer with a pH close to the pKa of the primary amine is recommended.By the method developed 32 amines with various structures were synthesized.
Preventive activities of N-substituted-α-aminonitriles against Fusarium diseases
Kirino,Oshita,Oishi,Kato
, p. 25 - 30 (2007/10/02)
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