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2-((benzyloxy)methyl)-2,3-dihydrofuran is an organic compound with the molecular formula C12H14O3. It is a colorless liquid with a molecular weight of 206.24 g/mol. 2-((benzyloxy)methyl)-2,3-dihydrofuran is characterized by a furan ring, which is a five-membered aromatic ring containing four carbon atoms and one oxygen atom. The 2-position of the furan ring is substituted with a benzyloxy group, which is a benzyl group (C6H5CH2-) attached to an oxygen atom. Additionally, the compound has a methylene group (-CH2-) at the 2-position, connecting the furan ring to the benzyloxy group. The 3-position of the furan ring is part of a dihydro structure, indicating that one of the double bonds in the furan ring has been reduced to a single bond. 2-((benzyloxy)methyl)-2,3-dihydrofuran is used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

16310-55-7

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16310-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16310-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,1 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16310-55:
(7*1)+(6*6)+(5*3)+(4*1)+(3*0)+(2*5)+(1*5)=77
77 % 10 = 7
So 16310-55-7 is a valid CAS Registry Number.

16310-55-7Relevant academic research and scientific papers

Cooperative Metal-Ligand Catalyzed Intramolecular Hydroamination and Hydroalkoxylation of Allenes Using a Stable Iron Catalyst

El-Sepelgy, Osama,Brzozowska, Aleksandra,Sklyaruk, Jan,Jang, Yoon Kyung,Zubar, Viktoriia,Rueping, Magnus

supporting information, p. 696 - 699 (2018/02/09)

A new iron-catalyzed chemoselective intramolecular hydroamination and hydroalkoxylation of the readily available α-allenic amines and alcohols to valuable unsaturated 5-membered heterocycles, 2,3-dihydropyrrole and 2,3-dihydrofuran, is reported. Effective

Ru- and Pd-catalysed synthesis of 2-arylfurans by one-flask heck arylation/oxidation

Schmidt, Bernd,Geissler, Diana

, p. 4814 - 4822 (2011/10/09)

2,5-Disubstituted furans were synthesized by one-flask Heck arylation/oxidation sequences. The starting materials are 2-substituted 2,3-dihydrofurans, conveniently available by RCM/isomerization sequences, and arenediazonium salts. These react in ligand-free Heck reactions to afford 2,5-disubstituted 2,5-dihydrofurans, which are oxidized to the corresponding furans without isolation or intermediate workup. The oxidation is conveniently achieved with chloranil or DDQ, depending on the substrate.

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