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5-N,N-dimethylaminomethyl-3-phenyl isoxazole is a chemical compound with the molecular formula C12H14N2O. It is a derivative of isoxazole, a heterocyclic organic compound consisting of a five-membered ring with one oxygen atom and one nitrogen atom. The compound features a 3-phenyl group attached to the isoxazole ring, which provides it with aromatic properties. Additionally, it has a 5-N,N-dimethylaminomethyl substituent, which consists of a nitrogen atom bonded to two methyl groups and a methylene group (-CH2-). This specific arrangement of functional groups endows the compound with unique chemical and physical properties, making it potentially useful in various applications, such as pharmaceuticals or agrochemicals.

1017-07-8

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1017-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1017-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1017-07:
(6*1)+(5*0)+(4*1)+(3*7)+(2*0)+(1*7)=38
38 % 10 = 8
So 1017-07-8 is a valid CAS Registry Number.

1017-07-8Downstream Products

1017-07-8Relevant academic research and scientific papers

Synthesis and properties of 3-alkyl(aryl)-5-chloromethylisoxazoles

Gadzhily,Aliev

, p. 415 - 418 (2007/10/03)

3-Chloro-2-isothiocyanato-1-propenyl alkyl(aryl) ketones react with hydroxylamine hydrochloride to give 3-alkyl(aryl)-5-chloromethylisoxazole. Treatment of the latter with dimethylamine and ammonium thiocyanate leads to formation of previously unknown 3-alkyl(aryl)-5-dimethylamino(or isothiocyanato)-methylisoxazoles.

Regioisomeric 5(3)-aminomethyl-3(5)-phenylisoxazoles: Synthesis, spectroscopic discrimination, and muscarinic activity

Dannhardt,Lambrecht,Laufer,Mutschler,Schweiger

, p. 437 - 443 (2007/10/02)

The regioselective synthesis of isomeric 5(3)-aminomethyl-3(5)-phenyl isoxazoles using different methods is described. Spectroscopic data, especially mass spectrometric fragmentation, were used to identify and characterize the regioisomers. The muscarinic

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