106588-24-3 Usage
Physical appearance
Clear, colorless liquid The compound is transparent and lacks color, making it difficult to see without proper lighting or background contrast.
Odor
Pungent 2-(methylamino)-butanenitrile has a strong, unpleasant smell that can be easily detected.
Usage
Pharmaceutical and organic compound synthesis The compound serves as an important intermediate in the production of various pharmaceuticals and organic compounds.
Applications
Pesticides, herbicides, and pharmaceutical drugs 2-(methylamino)-butanenitrile is commonly used in the production of these chemicals, which are essential in agriculture and healthcare.
Additional uses
Agrochemical synthesis and organic chemistry research The compound is also employed in the development of agrochemicals and as a research tool in the field of organic chemistry.
Reactivity
Highly reactive 2-(methylamino)-butanenitrile can easily undergo chemical reactions, making it important to handle with care.
Handling precautions
Potential hazards Due to its reactivity, 2-(methylamino)-butanenitrile can pose risks if not properly managed, and should be treated with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 106588-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 106588-24:
(8*1)+(7*0)+(6*6)+(5*5)+(4*8)+(3*8)+(2*2)+(1*4)=133
133 % 10 = 3
So 106588-24-3 is a valid CAS Registry Number.
106588-24-3Relevant articles and documents
The CSIC reaction on substrates derived from aldehydes
Marco, José L.,Ingate, Simon T.,Jaime, Carlos,Beá, Ivan
, p. 2523 - 2531 (2000)
The Carbanion-mediated Sulfonate (Sulfonamide) Intramolecular Cyclization reaction (CSIC reaction) on conveniently functionalized cyanoalkylsulfonates and cyanoalkylsulfonamides derived from aldehydes is possible and gives the new heterocyclic ring systems 5-alkyl-4-amino-5H-1,2- oxathiole 2,2-dioxide and 3-alkyl-5H-4-amino-5-cyano-5H-2,3- dihydroisothiazole 1,1-dioxide in good yield. (C) 2000 Elsevier Science Ltd.
Enzymatische Gewinnung enantiomerenreiner N-Alkyl-aminosaeuren
Groeger, Ulrich,Drauz, Karlheinz,Klenk, Herbert
, p. 222 - 224 (2007/10/02)
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