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Methanone, (5-butyl-4,5-dihydro-3-isoxazolyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92241-14-0

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92241-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92241-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92241-14:
(7*9)+(6*2)+(5*2)+(4*4)+(3*1)+(2*1)+(1*4)=110
110 % 10 = 0
So 92241-14-0 is a valid CAS Registry Number.

92241-14-0Downstream Products

92241-14-0Relevant academic research and scientific papers

Application of silica gel-supported polyphosphoric acid (PPA/SiO 2) as a reusable solid acid catalyst to the synthesis of 3-benzoylisoxazoles and isoxazolines

Itoh, Ken-Ichi,Aoyama, Tadashi,Satoh, Hiroaki,Fujii, Yuki,Sakamaki, Hiroshi,Takido, Toshio,Kodomari, Mitsuo

experimental part, p. 6892 - 6895 (2012/02/05)

3-Benzoylisoxazoles were synthesized by the reaction of alkynes and benzoylnitromethane using silica gel-supported polyphosphoric acid (PPA/SiO 2). This reaction provides a convenient, efficient, and reusable synthetic method of isoxazole deriv

Method for manufacturing isoxazole derivative or dihydroisoxazole derivative

-

Page/Page column 6, (2008/06/13)

There is provided with a method for manufacturing an isoxazole derivative at a high yield and without discharging waste products, and a novel isoxazole derivative. An isoxazole derivative expressed by Formula (8) is produced by reacting a 1-alkyne compoun

A convenient and efficient one-pot synthesis of 3-acylisoxazoles using iron(III) salts

Itoh, Ken-Ichi,Sakamaki, Hiroshi,Nakazato, Noriko,Horiuchi, Atsuo,Horn, Ernst,Horiuchi, C. Akira

, p. 3541 - 3548 (2007/10/03)

3-Acylisoxazoles were synthesized by the reaction of alkenes or alkynes with ketones (acetone or acetophenone), as both a reagent and the solvent, by three methods: iron(III) nitrate under reflux, iron(III) salt-nitrogen dioxide (NO2) at room temperature,

Formation of isoxazole derivatives via nitrile oxide using ammonium cerium nitrate (CAN): A novel one-pot synthesis of 3-acetyl- and 3-benzoylisoxazole derivatives

Itoh, Ken-Ichi,Horiuchi, C. Akira

, p. 1671 - 1681 (2007/10/03)

The reactions of alkenes and alkynes with ammonium cerium(IV) nitrate ((NH4)2Ce(NO3)6, CAN(IV)) in acetone under reflux gave the corresponding 3-acetyl-4,5-dihydroisoxazole and 3-acetylisoxazole derivatives. In the case of acetophenone, 3-benzoyl-4,5- dihydroisoxazole and 3-benzoylisoxazole derivatives were obtained. Reaction of acetone with CAN(IV) afforded the corresponding furoxan (3,4-diacetyl-1,2,5- oxadiazole 2-oxide) as the dimer of nitrile oxide. Moreover, it was found that yields of isoxazole derivatives were improved using ammonium cerium(III) nitrate tetrahydrate ((NH4)2Ce(NO3) 5·4H2O, CAN(III))-formic acid. The reaction mechanisms based on nitration and formation of nitrile oxide mediated by CAN(IV) or CAN(III) from acetone or acetophenone are also proposed.

Acid-Catalyzed Nitronate Cycloaddition Reactions. Useful Syntheses and Simple Transformations of 3-Acyl- and 3-Alkenylisoxazolines

Wade, Peter A.,Amin, Nayan V.,Yen, Hwa-Kwo,Price, David T.,Huhn, George F.

, p. 4595 - 4601 (2007/10/02)

Nitronic esters derived from primary nitro ketones, ethyl nitroacetate, and (phenylsulfonyl)nitromethane react with dipolarophiles in the presence of nonaqueous protic and Lewis acids to give nitrile oxide cycloadducts. α-Nitro ketones, ethyl nitroacetate

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