36687-98-6 Usage
Uses
Used in Industrial Applications:
2-Butanone, 3-methoxy-3-methyl(6CI,7CI,9CI) is used as a solvent due to its ability to dissolve a wide range of substances, making it suitable for various industrial processes.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-Butanone, 3-methoxy-3-methyl(6CI,7CI,9CI) serves as an important intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Perfumery:
2-Butanone, 3-methoxy-3-methyl(6CI,7CI,9CI) is utilized in the creation of perfumes, where it acts as a carrier for fragrances, helping to stabilize and prolong the scent.
Used in Flavor Industry:
2-Butanone, 3-methoxy-3-methyl(6CI,7CI,9CI) is also employed in the flavor industry to enhance and modify the taste profiles of various food and beverage products.
Safety Precautions:
Despite its low toxicity, 2-Butanone, 3-methoxy-3-methyl(6CI,7CI,9CI) can cause irritation to the eyes, skin, and respiratory system. Therefore, it is crucial to handle and store 2-Butanone, 3-methoxy-3-methyl- (6CI,7CI,9CI) with appropriate safety measures to minimize any adverse effects on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 36687-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36687-98:
(7*3)+(6*6)+(5*6)+(4*8)+(3*7)+(2*9)+(1*8)=166
166 % 10 = 6
So 36687-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-5(7)6(2,3)8-4/h1-4H3
36687-98-6Relevant articles and documents
STUDY OF THE INFLUENCING FACTORS ON THE REACTION OF α-HALOGENATED KETIMINES WITH CYANIDE ION
Kimpe, Norbert De,Sulmon, Paul,Schamp, Niceas
, p. 567 - 586 (2007/10/02)
The reaction of α-halogenated ketimines with cyanide ion in various solvents leads to α-cyanoaziridines.The scope and limitations of this reaction have been studied by investigating reaction parameters such as the nitrogen substituent, the solvent, the so
Formation of α-Cyanoaziridines and 1-(Alkylamino)cyclopropanecarbonitriles by Cyanation of α-Halo Ketimines
De Kimpe, Norbert,Sulmon, Paul,Verhe, Roland,De Buyck, Laurent,Schamp, Niceas
, p. 4320 - 4326 (2007/10/02)
A new convenient synthesis of α-cyanoaziridines was developed by reaction of α-halo ketimines with cyanide in methanol or acetonitrile.Tertiary α-chloro ketimines with cyanide in methanol gave rise to a competitive reaction between α-cyanoaziridine formation and production of 1-(alkylamino)cyclopropanecarbonitriles, the latter being classified as a Favorskii rearrangement-type product.The scope and limitations of this reaction have been determined by investigation of reaction parameters such as the nitrogen substituent, the solvent, the inorganic cyanide, the carbon skeleton, and the nature of the α-halogen.
