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Valeric acid-(4-fluoro-phenyl ester) is an organic compound that can be represented by the chemical formula C11H13FO2. It is an ester derivative of valeric acid, which is a saturated monocarboxylic acid with a five-carbon chain. In valeric acid-(4-fluoro-phenyl ester), the hydroxyl group of valeric acid is replaced by a 4-fluoro-phenyl group, resulting in an ester linkage. The 4-fluoro-phenyl group introduces a fluorine atom at the para position of the benzene ring, which can significantly influence the compound's reactivity and physical properties. This chemical is often used in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

351-90-6

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351-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351-90-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 351-90:
(5*3)+(4*5)+(3*1)+(2*9)+(1*0)=56
56 % 10 = 6
So 351-90-6 is a valid CAS Registry Number.

351-90-6Relevant academic research and scientific papers

Rhodium-Catalyzed Carbonylative Coupling of Alkyl Halides with Phenols under Low CO Pressure

Ai, Han-Jun,Li, Chong-Liang,Wang, Hai,Wu, Xiao-Feng

, p. 5147 - 5152 (2020)

A rhodium-catalyzed carbonylative transformation of alkyl halides under low pressure of CO has been developed. This robust catalyst system allows using phenols as the carbonylative coupling partner and, meanwhile, exhibits high functional group tolerance and good chemoselectivity. Substrates even with a large steric hindrance group or multiple reaction sites can be selectively converted into the desired products in good to excellent yields. A gram-scale experiment was performed and delivered an almost quantitative amount of the product. Control experiments were performed as well, and a possible reaction mechanism is proposed.

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