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1-Butoxy-2-nitro-4-(trifluoromethyl)benzene is an organic compound with the molecular formula C11H12F3NO3. It is a derivative of benzene, featuring a butoxy group (C4H9O) attached to the 1-position, a nitro group (NO2) at the 2-position, and a trifluoromethyl group (CF3) at the 4-position. This chemical is characterized by its aromatic structure, with the presence of electron-withdrawing nitro and trifluoromethyl groups, which can significantly influence its reactivity and physical properties. The compound may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals, and its specific applications would depend on its chemical reactivity and stability. Due to the presence of functional groups, it is important to handle 1-butoxy-2-nitro-4-(trifluoromethyl)benzene with care, as it may have potential health and environmental impacts.

787-34-8

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787-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 787-34-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 787-34:
(5*7)+(4*8)+(3*7)+(2*3)+(1*4)=98
98 % 10 = 8
So 787-34-8 is a valid CAS Registry Number.

787-34-8Downstream Products

787-34-8Relevant academic research and scientific papers

Synthesis of alkyl-aryl ethers by copper-catalyzed etherization reactions of aryl fluorides with tetraalkylammonium bromides and H2O

Wang, Feng,Tang, Boxiao,Xie, Yexiang,Li, Jinheng

experimental part, p. 2318 - 2322 (2011/10/03)

Synthesis of alkyl aryl ethers via copper-catalyzed etherizations of electron-deficient aryl fluorides with quaternary ammonium bromides and water has been developed. In the presence of Cu(OAc)2, POPh3 (L4) and Cs2CO3, a variety of electron-deficient aryl fluorides underwent the reaction with quaternary ammonium bromides and H 2O in moderate to good yields. The mechanism was also discussed. Synthesis of alkyl aryl ethers via copper-catalyzed etherizations of electron-deficient aryl fluorides with quaternary ammonium bromides and water has been developed. In the presence of Cu(OAc)2, POPh3 (L4) and Cs2CO3, a variety of electron-deficient aryl fluorides underwent the reaction with quaternary ammonium bromides and H 2O in moderate to good yields. Copyright

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