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α-Methyl-3-fluorohydrocinnamic acid is a chemical compound with the molecular formula C10H9FO2. It is a derivative of hydrocinnamic acid, featuring a fluorine atom at the 3rd carbon position and a methyl group at the α-carbon. This organic compound is characterized by its aromatic structure, with a phenyl ring attached to a three-carbon side chain that includes a double bond between the first and second carbons, making it a cinnamic acid analog. The presence of the fluorine atom imparts unique electronic and steric properties, which can significantly alter the compound's reactivity and physical characteristics compared to its non-fluorinated counterparts. α-methyl-3-fluorohydrocinnamic acid may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals where the introduction of fluorine can enhance biological activity or stability.

41201-57-4

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41201-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41201-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41201-57:
(7*4)+(6*1)+(5*2)+(4*0)+(3*1)+(2*5)+(1*7)=64
64 % 10 = 4
So 41201-57-4 is a valid CAS Registry Number.

41201-57-4Downstream Products

41201-57-4Relevant academic research and scientific papers

Palladium-Catalyzed C(sp3)-H Nitrooxylation with tert-Butyl Nitrite and Molecular Oxygen

Han, Ye-Qiang,Li, Bo,Shi, Bing-Feng,Yang, Xu

, p. 9719 - 9723 (2020)

Herein, we report a Pd(II)-catalyzed nitrooxylation of unactivated methyl C(sp3)-H bonds using commercial available and easily manageable tert-butyl nitrite as the precursor of ONO2 radical under aerobic conditions. Environmentally benign molecular oxygen is used to initiate the generation of active radical reactant; it is also used as the terminal oxidant. A broad range of nitrooxylated aliphatic carboxamides were prepared in moderate to good yields under mild conditions.

Chemical compounds and processes

-

, (2008/06/13)

Haloalkyl derivatives of aromatic compounds are prepared via reaction with dialkoxy or aralkoxy alkanes in the presence of a Lewis acid.

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