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3-methyl-2-[(1E)-2-phenylethenyl]quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133641-63-1

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133641-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133641-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,4 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133641-63:
(8*1)+(7*3)+(6*3)+(5*6)+(4*4)+(3*1)+(2*6)+(1*3)=111
111 % 10 = 1
So 133641-63-1 is a valid CAS Registry Number.

133641-63-1Downstream Products

133641-63-1Relevant academic research and scientific papers

Facile palladium-mediated substitution of chlorine in 2-chloroquinolines

Ciufolini, Marco A.,Mitchell, James W.,Roschangar, Frank

, p. 8281 - 8284 (1996)

Unlike ordinary aryl chlorides, the title heterocycles participate readily in Castro-Stephens, Stille, Suzuki, and carbonylation reactions under the catalytic influence of Pd(0).

NH4I-mediated sp3 C-H cross-dehydrogenative coupling of benzylamines with 2-methylquinoline for the synthesis of E-2-styrylquinolines

Huang, Bin,Li, Xue,Liao, WeiBo,Wang, JiangWei,Zhang, YuanYuan

, p. 903 - 910 (2021/07/17)

Without any metal catalyst, a simple and efficient method for the synthesis of E-2-styrylquinolines through sp3 C-H cross-dehydrogenative coupling of benzylamines with 2-methylquinolines mediated by NH4I under air is successfully developed. The oxidative olefination proceeded through deamination and sp3 C–H bond activation. A plausible mechanism is proposed for the construction of E-2-styrylquinolines.

Iodine-Catalyzed Direct C-H Alkenylation of Azaheterocycle N-Oxides with Alkenes

Zhang, Zhenhao,Pi, Chao,Tong, Heng,Cui, Xiuling,Wu, Yangjie

supporting information, p. 440 - 443 (2017/02/10)

An efficient and regioselective alkenylation of azaheterocycle N-oxides with alkenes catalyzed by iodine under metal- and external oxidant-free reaction conditions has been developed. A variety of (E)-2-styrylazaheterocycles have been produced in moderate

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