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Phenyl(3-phenyl-4,5-dihydroisoxazol-5-yl)methanol is a complex organic compound with the molecular formula C17H15NO2. It is characterized by a phenyl group attached to a 3-phenyl-4,5-dihydroisoxazol-5-yl moiety, which features a five-membered isoxazole ring fused to a dihydroisoxazole ring. phenyl(3-phenyl-4,5-dihydroisoxazol-5-yl)methanol is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other bioactive molecules, due to its unique structure and potential reactivity. The compound's properties, such as its solubility, stability, and potential applications, are areas of ongoing research and development.

2126-00-3

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2126-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2126-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2126-00:
(6*2)+(5*1)+(4*2)+(3*6)+(2*0)+(1*0)=43
43 % 10 = 3
So 2126-00-3 is a valid CAS Registry Number.

2126-00-3Downstream Products

2126-00-3Relevant academic research and scientific papers

Green organocatalytic synthesis of isoxazolines via a one-pot oxidation of allyloximes

Triandafillidi, Ierasia,Kokotos, Christoforos G.

, p. 106 - 109 (2017/11/27)

A green, sustainable, organocatalytic, and efficient synthesis of isoxazolines from allyloximes was developed. A 2,2,2-trifluoroacetophenone-catalyzed oxidation of allyloximes, utilizing H2O2 as the green oxidant, was taken advantage of in order to introduce a cheap and environmentally friendly protocol for the synthesis of substituted isoxazolines. A variety of substitution patterns, both aromatic and aliphatic moieties, are well tolerated, leading to isoxazolines in moderate to excellent yields.

Organophotocatalytic Generation of N- and O-Centred Radicals Enables Aerobic Oxyamination and Dioxygenation of Alkenes

Hu, Xiao-Qiang,Chen, Jun,Chen, Jia-Rong,Yan, Dong-Mei,Xiao, Wen-Jing

supporting information, p. 14141 - 14146 (2016/09/23)

A cooperative TEMPO and photoredox catalytic strategy was applied for the first time to the direct conversion of N?H and O?H bonds into N- and O-centred radicals, enabling a general and selective oxidative radical oxyamination and dioxygenation of various

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