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2,2,5-Trimethyl-5-phenyl-2,5-dihydro-furan is an organic compound characterized by a unique molecular structure. It features a furan ring, which is a five-membered aromatic ring containing four carbon atoms and one oxygen atom. The compound is further distinguished by the presence of three methyl groups (CH3) at the 2nd and 5th positions of the furan ring, and a phenyl group (C6H5) attached to the 5th carbon. This phenyl group is a benzene ring, which contributes to the compound's aromatic properties. The "2,5-dihydro" part of the name indicates that the furan ring is partially saturated, meaning it has two hydrogen atoms added across one of the double bonds in the furan ring, making it a dihydro derivative. 2,2,5-trimethyl-5-phenyl-2,5-dihydro-furan is of interest in organic chemistry and may have applications in the synthesis of various pharmaceuticals and other chemical products due to its complex ring structure and substituents.

58607-52-6

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58607-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58607-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58607-52:
(7*5)+(6*8)+(5*6)+(4*0)+(3*7)+(2*5)+(1*2)=146
146 % 10 = 6
So 58607-52-6 is a valid CAS Registry Number.

58607-52-6Downstream Products

58607-52-6Relevant academic research and scientific papers

Arylative Allenol Cyclization via Sequential One-pot Enzyme & Palladium Catalysis

Naapuri, Janne M.,?berg, Gustav A.,Palomo, Jose M.,Deska, Jan

, p. 763 - 769 (2021)

The one-pot combination of halogenation biocatalysis and Suzuki-type cross coupling enables the direct arylative cyclization of allenic alcohols with boronic acids. This modular approach to unsaturated five-membered O-heterocycles proceeds in an aqueous emulsion with air as terminal oxidant. Here, the enzymatic oxidative activation of simple halide salts acts as traceless ring-closure-inducing event to trigger the subsequent C?C coupling. With the original protocol merging soluble proteins and a homogeneous SPhos-based palladium catalyst as a template, a novel heterogeneous nanobiohybrid was developed. Consisting of an oxidase matrix hosting small spherical palladium nanoparticles, this enzyme-metal hybrid exhibits catalytic competence for both the biocyclization as well as the C?C bond-forming cross coupling, underlining the potential of this new techniques for streamlining chemoenzymatic approaches.

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