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2-Methoxycyclohexanone oxime is an organic compound with the molecular formula C7H13NO2. It is a derivative of cyclohexanone, featuring a methoxy group (-OCH3) at the 2-position and an oxime group (-NHOH) attached to the carbonyl carbon. 2-methoxycyclohexanone oxime is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. The oxime group in 2-methoxycyclohexanone oxime is significant because it can undergo further chemical reactions, such as the formation of oxime ethers or the Beckmann rearrangement, which can lead to the synthesis of amines. The compound is typically synthesized through the reaction of 2-methoxycyclohexanone with hydroxylamine, and its structure and properties make it a valuable building block in organic chemistry.

3307-32-2

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3307-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3307-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3307-32:
(6*3)+(5*3)+(4*0)+(3*7)+(2*3)+(1*2)=62
62 % 10 = 2
So 3307-32-2 is a valid CAS Registry Number.

3307-32-2Relevant academic research and scientific papers

NANOMATERIALS

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Paragraph 0460-0462, (2021/07/17)

Lipid nanoparticle compositions for delivery of nucleic acids are described. In various embodiments the lipid nanoparticle contains an ionizable lipid of the Formula (I). Methods of using such lipid nanoparticle compositions to achieve targeted delivery of therapeutic cargo without the need for a targeting ligand are also provided.

Organic Synthesis Utilizing Beckmann Fragmentation: New Carbon-Carbon Bond Formation by the Reaction of α-Alkoxycycloalkanone Oxime Acetates with Organoaluminium Reagents

Fujioka, Hiromichi,Yamanaka, Takeshi,Takuma, Kazuhiro,Miyazaki, Makoto,Kita, Yasuyuki

, p. 533 - 534 (2007/10/02)

The reaction of α-alkoxycycloalkanone oxime acetates 1 with organoaluminium reagents caused Beckmann fragmentation and subsequent carbon-carbon bond formation to give various types of ω-cyano-α-alkyl (or alkynyl)ethers 2 in high yields.

Beckmann fragmentation and successive carbon-carbon bond formation of α-alkoxycycloalkanone oximes catalyzed by trimethylsilyl trifluoromethanesulfonate

Fujioka,Miyazaki,Yamanaka,Yamamoto,Kita

, p. 5951 - 5954 (2007/10/02)

Title reaction occurred in the presence of silicon-containing carbon nucleophiles and various types of functionalized ω-nitrile compounds were obtained from the oximes in one-pot operation.

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