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2,3-Dimethyl-4-phenyl-furan is an organic compound with the chemical formula C??H??O. It is a derivative of furan, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In this specific compound, two methyl groups (-CH?) are attached to the second and third carbon atoms of the furan ring, while a phenyl group (C?H?) is connected to the fourth carbon atom. This chemical is known for its unique aroma and is used as a flavoring agent in the food and beverage industry, as well as a fragrance component in the perfumery sector. It is also found in various natural products, such as essential oils and some fruits. Due to its chemical structure, 2,3-dimethyl-4-phenyl-furan exhibits properties that make it a valuable compound in the synthesis of pharmaceuticals and other organic compounds.

5109-66-0

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5109-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5109-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5109-66:
(6*5)+(5*1)+(4*0)+(3*9)+(2*6)+(1*6)=80
80 % 10 = 0
So 5109-66-0 is a valid CAS Registry Number.

5109-66-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-4-phenylfuran

1.2 Other means of identification

Product number -
Other names Furan,2,3-dimethyl-4-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5109-66-0 SDS

5109-66-0Downstream Products

5109-66-0Relevant academic research and scientific papers

Direct β-arylation of furans with aryl iodides catalyzed by dinuclear palladium complexes

Goto, Takahiro,Kato, Hayate,Tsukada, Naofumi

, p. 2222 - 2228 (2017/12/12)

Dinuclear palladium complexes formed by a chelate-bridging ligand showed β-selectivity in the direct arylation of furans with iodoarenes. In contrast, the arylation using PPh3 or bpy as ligands gave α-arylfurans as major products. The arylation

Indium-mediated allenylation of arylacyl bromides in a route for the synthesis of substituted furans

Lin, Mei-Huey,Kuo, Chung-Kai,Huang, Yen-Chih,Tsai, Yu-Ting,Tsai, Chang-Hsien,Liang, Kung-Yu,Li, Yi-Syuan,Chuang, Tsung-Hsun

, p. 5513 - 5518 (2015/03/30)

A three-step, single purification procedure has been developed for the concise synthesis of substituted furans from arylacyl bromides.

Reaction of Tributyltin Enolates with α-Halogeno Ketones: a New Route to Furan Derivatives

Kosugi, Masanori,Takano, Izumi,Hoshino, Isao,Migita, Toshihiko

, p. 989 - 990 (2007/10/02)

The reaction of tributyltin enolates with α-halogeno ketones gave substituted furans which were not derived from the normal cross-coupling products, 1,4-diketones, but were formed instead through addition of the tin enolate to the α-halogeno ketones.

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