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1H-Pyrazole, 5-(2-chlorophenyl)-4,5-dihydro-3-(4-methoxyphenyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

489398-73-4

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489398-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 489398-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,9,3,9 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 489398-73:
(8*4)+(7*8)+(6*9)+(5*3)+(4*9)+(3*8)+(2*7)+(1*3)=234
234 % 10 = 4
So 489398-73-4 is a valid CAS Registry Number.

489398-73-4Downstream Products

489398-73-4Relevant academic research and scientific papers

Silica-supported synthesis of some 1,3,5-trisubstituted 2-pyrazolines under solvent-free and microwave irradiation conditions

Azarifar, Davood,Maleki, Behrooz

, p. 157 - 159 (2005)

A simple method for the synthesis of 2-pyrazolines is described which occurs on silica surface under solvent-free conditions within 110-180 sec using microwave irradiation. The results obtained indicate that the use of silica gel as a support in pyrazolin

Novel synthesis of 1,3,5-trisubstituted 2-pyrazolines promoted by chlorotrimethylsilane

Xie, Zengyang,Bian, Xiaoqin,Geng, Xin,Li, Shuangshuang,Wang, Cunde

, p. 52 - 54 (2008/09/19)

1,3,5-Trisubstituted-2-pyrazolines were effectively synthesised by utilising chlorotrimethylsilane as an efficient promoter in the cyclisation addition of Phenylhydrazine to chalcones under nitrogen in acetonitrile. The clean, mild reaction conditions, high yields and a simple workup of target compounds were attractive features of the reaction which enables a facile preparative procedure for building the pyrazoline ring.

Convenient synthesis of highly functionalized pyrazolines via mild, photoactivated 1,3-dipolar cycloaddition

Wang, Yizhong,Rivera Vera, Claudia I.,Lin, Qing

, p. 4155 - 4158 (2008/02/12)

A mild, photoactivated 1,3-dipolar cycloaddition procedure was successfully developed for the synthesis of polysubstituted pyrazolines. This procedure involved the in situ generation of the reactive nitrile imine dipoles using a hand-held UV lamp at 302 n

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