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1-(1H-1,3-imidazol-1-yl)2-phenyl-ethen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

339549-16-5

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339549-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 339549-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,5,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 339549-16:
(8*3)+(7*3)+(6*9)+(5*5)+(4*4)+(3*9)+(2*1)+(1*6)=175
175 % 10 = 5
So 339549-16-5 is a valid CAS Registry Number.

339549-16-5Downstream Products

339549-16-5Relevant academic research and scientific papers

Transition-metal-free synthesis of N-(1-Alkenyl)imidazoles by potassium phosphate-promoted addition reaction of alkynes to imidazoles

Lu, Linhua,Yan, Hong,Liu, Defu,Rong, Guangwei,Mao, Jincheng

supporting information, p. 75 - 78 (2014/01/06)

The addition reaction of alkynes to N-heterocycles by simply heating in DMSO with potassium phosphate is reported. Good yields with high stereoselectivity could be achieved for a range of substrates. The scope is quite general for both amines and phenylac

ORGANISCHE PHOSPHORVERBINDUNGEN 81. HERSTELLUNG VON HETEROCYCLISCH SUBSTITUIERTEN PHOSPHINOXIDEN UND DEREN VERWENDUNG IN DER WITTIG-HORNER REAKTION

Maier, Ludwig,Rist, G.

, p. 65 - 72 (2007/10/02)

The reaction of dimethyl-chloromethylphosphinoxide with the alkali salts of imidazole, pyrazole, triazole, benztriazole, 2-methylimidazole, benzimidazole, tetrazole, and indazole yields the corresponding dimethyl-heterocyclic substituted methylphosphine oxides 1a-1i.These phosphine oxides easily undergo a Wittig-Horner reaction when treated with aldehydes and ketones and give a cis/trans = 1:1 mixture of the corresponding olefines 2a, 2a', 2b, 2d and 2f.Several of these can be separated by flash chromatography into the pure cis and trans isomers.It was observed that only the cis compounds exhibit fungicidal activity against Erysiphe graminis.

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