57134-36-8 Usage
Physical appearance
Clear, colorless liquid
1-methoxyhexan-2-one is a transparent liquid without any color, making it difficult to see.
Odor
Sweet, fruity
This compound has a pleasant and aromatic smell, reminiscent of sweet fruits.
Uses
Solvent in paints, coatings, and adhesives
Due to its chemical properties, 1-methoxyhexan-2-one is commonly used as a solvent in the production of various materials, such as paints, coatings, and adhesives.
Synthesis
Organic compounds and pharmaceuticals
This compound is also used as a starting material or reagent in the synthesis of other organic compounds and pharmaceuticals, making it valuable in the chemical industry and research.
Reactivity
Ability to undergo various chemical reactions
1-methoxyhexan-2-one is known for its reactivity, allowing it to participate in a wide range of chemical reactions, which contributes to its versatility and usefulness in industrial and research applications.
Safety concerns
Flammability, potential health hazards
While 1-methoxyhexan-2-one is a useful compound, it should be handled with caution due to its flammability and potential health hazards if not used properly in a controlled environment.
Check Digit Verification of cas no
The CAS Registry Mumber 57134-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57134-36:
(7*5)+(6*7)+(5*1)+(4*3)+(3*4)+(2*3)+(1*6)=118
118 % 10 = 8
So 57134-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-3-4-5-7(8)6-9-2/h3-6H2,1-2H3
57134-36-8Relevant articles and documents
New general synthesis of α-alkoxyketones via α′- alkylation, α-alkylation and α,α′-dialkylation of α-alkoxyketimines
Colpaert, Filip,Mangelinckx, Sven,Rocchetti, Maria Teresa,De Kimpe, Norbert
experimental part, p. 549 - 558 (2011/02/28)
α-Methoxy- and α-ethoxyketones, as important intermediates in organic synthesis and flavor compounds in food chemistry, were synthesized by deprotonation of N-(1-alkoxy-2-propylidene)isopropylamine, prepared by condensation of the corresponding α-alkoxyacetone with isopropylamine, and subsequent reaction of the corresponding 1-azaallylic anions with alkyl halides to afford α′-alkylated, α-alkylated and α, α′-dialkylated ketimines. Hydrolysis of the imino function led to the desired substituted α-alkoxyketones. The ratio of α-, α′-, and α,α′-(di)alkylated compounds depended on the amount of base used and on the nature of the alkylating reagent.
A NEW SYNTHETIC METHOD FOR 1-METHOXY-2-ALKANONES FROM 1,2-DIMETHOXYETHENYLLITHIUM AND ORGANOBORANES
Koshino, Junji,Sugawara, Takahiro,Yogo, Toshinobu,Suzuki, Akira
, p. 933 - 934 (2007/10/02)
1-Methoxy-2-alkanones are prepared from ate-complexes formed from 1,2-dimethoxyethenyllithium and trialkylboranes by the reaction with BF3*Et2O, followed by basic hydrogen peroxide oxidation.
