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Benzene, 1-[(1E)-2-bromo-2-fluoroethenyl]-4-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

459132-91-3

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459132-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 459132-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,1,3 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 459132-91:
(8*4)+(7*5)+(6*9)+(5*1)+(4*3)+(3*2)+(2*9)+(1*1)=163
163 % 10 = 3
So 459132-91-3 is a valid CAS Registry Number.

459132-91-3Downstream Products

459132-91-3Relevant academic research and scientific papers

A simple, two-step, site-specific preparation of fluorinated naphthalene and phenanthrene derivatives from fluorobromo-substituted alkenes

Wang, Yi,Xu, Jianjun,Burton, Donald J.

, p. 7780 - 7784 (2006)

(Chemical Equation Presented) A facile two-step procedure for the site-specific preparation of fluorinated naphthalene and phenanthrene derivatives is described. The Sonogashira reaction of bromofluoro-substituted alkenes with terminal alkynes, followed b

Reactions of carbonyl compounds with phosphorus ylide generated from tribromofluoromethane and tris(dimethylamino)phosphine

Hirai, Go,Nishizawa, Eri,Kakumoto, Daiki,Morita, Masaki,Okada, Mitsuaki,Hashizume, Daisuke,Nagashima, Sayoko,Sodeoka, Mikiko

supporting information, p. 1389 - 1391 (2015/11/17)

The reactions of fluorinated ylide, generated from tris(dimethylamino) phosphine and tribromofluoromethane, with simple aldehydes and reactive ketones gave the expected Wittig reaction products. However, a ketone having a galactose skeleton afforded an acid fluoride, probably through an unprecedented CoreyChaykovski- type epoxide formation reaction, followed by spontaneous Meinwald rearrangement.

A facile and mild method for the synthesis of terminal bromofluoroolefins via diethylzinc-promoted wittig reaction

Lei, Xinsheng,Dutheuil, Guillaume,Pannecoucke, Xavier,Quirion, Jean-Charles

, p. 2101 - 2104 (2007/10/03)

Synthesis of 1-bromo-1-fluoroolefins was achieved in good yields via a Wittig reaction promoted by diethylzinc, even with nonactivated aldehydes and ketones as starting materials.

Stereospecific preparation of (Z)-α-fluorostilbenes via a kinetically controlled palladium-catalyzed cross-coupling reaction of high E/Z ratio 1-bromo-1-fluorostyrenes and aryl stannanes

Xu, Jianjun,Burton, Donald J

, p. 2877 - 2879 (2007/10/03)

High E/Z ratios were obtained for 1-bromo-1-fluorostyrenes by isomerization from the original E/Z ratios of approximately 1:1. The palladium-catalyzed cross-coupling reaction of high E/Z ratio 1-bromo-1-fluorostyrenes with aryl stannanes gives (Z)-α-fluor

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