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5-ethyl-3-phenyl-4,5-dihydroisoxazol-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

449181-06-0

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449181-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 449181-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,1,8 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 449181-06:
(8*4)+(7*4)+(6*9)+(5*1)+(4*8)+(3*1)+(2*0)+(1*6)=160
160 % 10 = 0
So 449181-06-0 is a valid CAS Registry Number.

449181-06-0Downstream Products

449181-06-0Relevant academic research and scientific papers

Complementary regioselective synthesis of 3,5-disubstituted isoxazoles from ynones

Liu, Xiaochen,Hong, Dongsub,She, Zhigang,Hersh, William H.,Yoo, Barney,Chen, Yu

, p. 6593 - 6606 (2018/10/05)

Two regioselective synthetic routes towards 3,5-disubstituted isoxazoles from ynones are reported. One route takes place via first converting the ynones to ynone O-methyl oximes, followed by a palladium-catalyzed intramolecular cyclization. The other invo

Preparation of 3,5-disubstituted pyrazoles and isoxazoles from terminal alkynes, aldehydes, hydrazines, and hydroxylamine

Harigae, Ryo,Moriyama, Katsuhiko,Togo, Hideo

, p. 2049 - 2058 (2014/04/03)

The reaction of terminal alkynes with n-BuLi, and then with aldehydes, followed by the treatment with molecular iodine, and subsequently hydrazines or hydroxylamine provided the corresponding 3,5-disubstituted pyrazoles or isoxazoles in good yields with high regioselectivity, through the formations of propargyl secondary alkoxides and α-alkynyl ketones. The present reactions are one-pot preparation of 3,5-disubstituted pyrazoles from terminal alkynes, aldehydes, molecular iodine, and hydrazines, and 3,5-disubstituted isoxazoles from terminal alkynes, aldehydes, molecular iodine, and hydroxylamine.

Regioselective synthesis and side-chain metallation and elaboration of 3-aryl-5-alkylisoxazoles

Di Nunno, Leonardo,Scilimati, Antonio,Vitale, Paola

, p. 2659 - 2665 (2007/10/03)

A number of 3-aryl-5-alkylisoxazoles have been synthesized in high yields by reacting arylnitrile oxides with free enolate ions regioselectively obtained by metallation of various alkyl methyl ketones with LDA in THF at -78°C followed by dehydration. Inve

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