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(Z)-1-(3-methoxyphenyl)-3-phenylprop-2-yn-1-one O-methyl oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1365162-67-9

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1365162-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1365162-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,1,6 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1365162-67:
(9*1)+(8*3)+(7*6)+(6*5)+(5*1)+(4*6)+(3*2)+(2*6)+(1*7)=159
159 % 10 = 9
So 1365162-67-9 is a valid CAS Registry Number.

1365162-67-9Relevant 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

Direct synthesis of 4-fluoroisoxazoles through gold-catalyzed cascade cyclization-fluorination of 2-alkynone O-methyl oximes

Jeong, Yunkyung,Kim, Bom-I,Lee, Jae Kyun,Ryu, Jae-Sang

, p. 6444 - 6455 (2014/08/05)

A tandem protocol for the synthesis of fluorinated isoxazoles has been developed via catalytic intramolecular cyclizations of 2-alkynone O-methyl oximes and ensuing fluorination. The reactions proceed smoothly at room temperature in the presence of 5 mol

Synthesis of trisubstituted isoxazoles by palladium(ii)-catalyzed cascade cyclization-alkenylation of 2-alkyn-1-one o -methyl oximes

She, Zhigang,Niu, Dongyue,Chen, Lei,Gunawan, Maria A.,Shanja, Xhesika,Hersh, William H.,Chen, Yu

, p. 3627 - 3633 (2012/06/15)

A palladium-catalyzed, cascade 5-endo-dig cyclization-alkenylation synthesis of isoxazoles has been developed. The addition of 1 equiv of n-Bu 4NBr significantly increases the yield of the desired 4-alkenyl-3,4,5-trisubstituted isoxazoles. A va

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