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2-Furancarboxylic acid, 5-(4-methoxyphenyl)-, ethyl ester is a chemical compound that belongs to the class of furan carboxylic acids. It is a derivative of furan carboxylic acid with a 4-methoxyphenyl group attached to the 5-position and an ethyl ester group.
Used in Pharmaceutical Industry:
2-Furancarboxylic acid, 5-(4-methoxyphenyl)-, ethyl ester is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique chemical properties and reactivity make it a promising candidate for the development of new drugs.
Used in Agrochemical Industry:
2-Furancarboxylic acid, 5-(4-methoxyphenyl)-, ethyl ester is also used as a chemical intermediate in the synthesis of agrochemicals. Its potential applications in this industry may include the development of new pesticides or other agricultural chemicals.
Used in Other Industries:
Due to its unique chemical properties and reactivity, 2-Furancarboxylic acid, 5-(4-methoxyphenyl)-, ethyl ester may have other industrial applications that require further research to fully understand its potential uses and effects.

60336-07-4

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60336-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60336-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,3 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60336-07:
(7*6)+(6*0)+(5*3)+(4*3)+(3*6)+(2*0)+(1*7)=94
94 % 10 = 4
So 60336-07-4 is a valid CAS Registry Number.

60336-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-(4-methoxyphenyl)furan-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Furancarboxylic acid,5-(4-methoxyphenyl)-,ethyl ester

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:60336-07-4 SDS

60336-07-4Downstream Products

60336-07-4Relevant academic research and scientific papers

Triflic Acid-Catalyzed Cycloisomerization Reactions of Donor-Acceptor Cyclopropanes: Access to Alkyl 5-Arylfuran-2-carboxylates

Zhu, Yuequan,Xu, Panpan,Gong, Yuefa

, p. 4829 - 4834 (2016/07/06)

A direct synthetic strategy starting from alkyl 1-alkoxy-2-aroylcyclopropanecarboxylates was developed for the construction of alkyl 5-arylfuran-2-carboxylates. These donor-acceptor cyclopropanes smoothly undergo a simple ring-opening reaction or/and cycl

Mono- and biscouplings using triarylbismuths for the atom-efficient arylations of functionalized furans under palladium catalysis

Rao, Maddali L. N.,Awasthi, Dheeraj K.,Talode, Jalindar B.

supporting information; experimental part, p. 1907 - 1912 (2012/09/22)

Palladium-catalyzed cross-coupling reactions of functionalized bromofurans with triarylbismuths have been described for the atom-economic synthesis of functionalized arylfuran systems. The coupling reactions using triarylbismuths with various 2-bromofurans and 2,5-dibromofuran underwent smoothly to afford the corresponding 2-arylfurans and 2,5-diarylfurans in high yields in a short reaction time (one hour). Georg Thieme Verlag Stuttgart · New York.

Cobalt-catalyzed cross-coupling reactions of heterocyclic chlorides with arylmagnesium halides and of polyfunctionalized arylcopper reagents with aryl bromides, chlorides, fluorides and tosylates

Korn, Tobias J.,Schade, Matthias A.,Cheemala, Murthy N.,Wirth, Stefan,Guevara, Simon A.,Cahiez, Gerard,Knochel, Paul

, p. 3547 - 3574 (2008/03/14)

A range of aromatic organocopper or organomagnesium compounds undergo smooth cross-coupling reactions with aryl bromides, chlorides, fluorides and tosylates, leading to polyfunctionalized aromatics or heterocycles in the presence of cobalt salts (5-7.5 mol%) as catalysts. Very mild reaction conditions are needed and, in the case of cross-coupling with organocopper compounds, Bu4NI (1 equiv) and 4-fluorostyrene (20 mol%) are essential as promoters for successful couplings. Georg Thieme Verlag Stuttgart.

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