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Dimethyl 4,5-diphenylfuran-2,3-dicarboxylate is a chemical compound with the molecular formula C18H14O4. It is a derivative of furan, a heterocyclic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In this specific compound, the furan ring is substituted with two phenyl groups at the 4 and 5 positions, and two ester groups are attached to the 2 and 3 positions, with each ester group containing a methyl group. dimethyl 4,5-diphenylfuran-2,3-dicarboxylate is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving furan, phenyl groups, and esterification processes.

1048-83-5

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1048-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1048-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1048-83:
(6*1)+(5*0)+(4*4)+(3*8)+(2*8)+(1*3)=65
65 % 10 = 5
So 1048-83-5 is a valid CAS Registry Number.

1048-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4,5-diphenylfuran-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4,5-Diphenyl-furan-dicarbonsaeure-dimethylester-(2,3)

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:1048-83-5 SDS

1048-83-5Relevant academic research and scientific papers

Synthesis of multisubstituted furans via Cu(i)-catalyzed annulation of ketones with alkynoate under ligand- and additive-free conditions

Luo, Zaigang,Fang, Yuyu,Zhao, Yu,Liu, Peng,Xu, Xuemei,Feng, Chengtao,Li, Zhong,He, Jie

, p. 5436 - 5441 (2016/02/05)

A facile and efficient annulation strategy for the synthesis of multisubstituted furan derivatives has been achieved under mild conditions. The developed transformation via C(sp3)-H bond functionalization catalyzed by copper(i) salts using benz

An efficient and general iron-catalyzed one-pot synthesis of furans via α-hydroxy ketones and activated alkynes

Cao, Hua,Zhan, Haiying,Wu, Jianyong,Zhong, Haiping,Lin, Yuanguang,Zhang, Hong

, p. 2318 - 2322 (2012/05/19)

A new practical and economical process for the synthesis of substituted furan derivatives has been developed by an FeCl3-catalyzed reaction of α-hydroxy ketones with activated alkynes. This methodology represents a highly efficient synthetic route to electron-deficient furans for which catalytic approaches are scarce. Furthermore, this transformation is associated with readily available substrates, good yields, and mild conditions. An efficient iron-catalyzed one-pot synthesis of polysubstituted furans has been developed from electron-deficient alkynes and α-hydroxy ketones under mild reaction conditions. This green and eco-friendly system has shown high catalytic activity in the synthesis of furan derivatives. The yields are good, and the scope of substrates is wide.

CuO/CNTs-catalyzed heterogeneous process: A convenient strategy to prepare furan derivatives from electron-deficient alkynes and α-hydroxy ketones

Cao, Hua,Jiang, Huan-Feng,Zhou, Xiao-Song,Qi, Chao-Rong,Lin, Yuan-Guang,Wu, Jian-Yong,Liang, Qi-Mei

, p. 2710 - 2714 (2012/11/07)

As heterogeneous catalysts and nanoparticle support materials, CNTs have attracted great interest in organic chemistry. This paper reports facile CuO/CNTs-catalyzed cyclization to form furan derivatives from electron-deficient alkynes and α-hydroxy ketones. It represents a facile synthetic route, and the eco-friendly catalyst can be easily separated by filtration and reused.

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