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2-AMINO-4,5-BIS(4-METHOXYPHENYL)FURAN-3& is a chemical compound characterized by a furan-based structure with two amino groups and two methoxyphenyl groups. This unique molecular configuration endows it with potential applications in materials science and pharmaceuticals, making it a subject of interest for research and development.
Used in Pharmaceutical Industry:
2-AMINO-4,5-BIS(4-METHOXYPHENYL)FURAN-3& is used as a building block for the synthesis of heterocyclic compounds due to its amino and methoxyphenyl groups, which may contribute to biological activity.
Used in Materials Science:
2-AMINO-4,5-BIS(4-METHOXYPHENYL)FURAN-3& is used as a component in the development of new materials, leveraging its unique structure and properties to enhance material performance.

94556-80-6

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94556-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94556-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94556-80:
(7*9)+(6*4)+(5*5)+(4*5)+(3*6)+(2*8)+(1*0)=166
166 % 10 = 6
So 94556-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H16N2O3/c1-22-14-7-3-12(4-8-14)17-16(11-20)19(21)24-18(17)13-5-9-15(23-2)10-6-13/h3-10H,21H2,1-2H3

94556-80-6 Well-known Company Product Price

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  • Aldrich

  • (573027)  2-Amino-4,5-bis(4-methoxyphenyl)furan-3-carbonitrile  97%

  • 94556-80-6

  • 573027-1G

  • 1,230.84CNY

  • Detail

94556-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4,5-bis(4-methoxyphenyl)furan-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-amino-4,5-di-p-anisyl-3-furonitrile

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:94556-80-6 SDS

94556-80-6Relevant academic research and scientific papers

Identification, SAR studies, and X-ray Co-crystallographic analysis of a novel furanopyrimidine aurora kinase a inhibitor

Coumar, Mohane Selvaraj,Tsai, Ming-Tsung,Chu, Chang-Ying,Uang, Biing-Jiun,Lin, Wen-Hsing,Chang, Chun-Yu,Chang, Teng-Yuan,Leou, Jiun-Shyang,Teng, Chi-Huang,Wu, Jian-Sung,Fang, Ming-Yu,Chen, Chun-Hwa,Hsu, John T.-A.,Wu, Su-Ying,Chao, Yu-Sheng,Hsieh, Hsing-Pang

experimental part, p. 255 - 267 (2010/12/18)

Herein we reveal a simple method for the identification of novel Aurora kinase A inhibitors through substructure searching of an in-house compound library to select compounds for testing. A hydrazone fragment conferring Aurora kinase activity and heterocy

COMPOUND FOR INHIBITING TYROSINE KINASE ACTIVITY OF DDR2 PROTEIN

-

Page/Page column 35-36, (2010/02/14)

A new furopyrimidine compound, their pharmaceutically acceptable salt, and a tyrosine kinase activity inhibitor. The furopyrimidine compound is a compound defined by chemical formula 1, 2, 3 or 4, on their precursor, and can exist as a form of free base or in an acid-addition salt. Since the furopyrimidine compound has an effect of inhibiting activity of DDR2 tyrosine kinase, it can be used in treating illnesses caused by the DDR2 tyrosine kinase activity such as hepatocirrhosis, rheumatoid arthritis or cancer.

First Synthesis of 4H-Furo[3,2-f]pyrrolo[1,2-a][1,4]diazepines

Feng, Xiao,Lancelot, Jean-Charles,Prunier, Herve,Rault, Sylvain

, p. 2007 - 2011 (2007/10/03)

The synthetic pathway leading to 4-H-furo[3,2-f]pyrrolo[1,2-a][1,4]diazepines is described in five steps starting from 2-hydroxyketones via 2-amino-3-furonitriles.

Ring Transformation and Reactions of 2-Amino-4,5-dihydrofuran-3,4-dicarbonitriles

Aran, Vincente J.,Perez, Miguel A.,Soto, Jose L.

, p. 2009 - 2011 (2007/10/02)

The 2-amino-4,5-dihydrofuran-3,4-dicarbonitriles (1a-f) were thermally aromatized to the 2-aminofuran-3-carbonitriles (2a-f) which, in turn, underwent photoxidative ring transformation into the 2,5-dihydro-5-hydroxy-2-oxopyrrole-3-carbonitriles (3b-e).Mil

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