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54802-10-7

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54802-10-7 Usage

General Description

3-Aminobenzofuran-2-carboxamide 97 is a chemical compound with the molecular formula C9H9N3O2. It is a derivative of benzofuran and contains an amine and amide functional group. 3-AMINOBENZOFURAN-2-CARBOXAMIDE 97 is commonly used in the synthesis of pharmaceuticals and as an intermediate in the production of various organic compounds. It can also act as a building block for the construction of more complex molecules. The 97 designation indicates that the compound has a high level of purity, making it suitable for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 54802-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54802-10:
(7*5)+(6*4)+(5*8)+(4*0)+(3*2)+(2*1)+(1*0)=107
107 % 10 = 7
So 54802-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c10-7-5-3-1-2-4-6(5)13-8(7)9(11)12/h1-4H,10H2,(H2,11,12)

54802-10-7 Well-known Company Product Price

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  • Aldrich

  • (631523)  3-Aminobenzofuran-2-carboxamide  97%

  • 54802-10-7

  • 631523-1G

  • 458.64CNY

  • Detail
  • Aldrich

  • (631523)  3-Aminobenzofuran-2-carboxamide  97%

  • 54802-10-7

  • 631523-5G

  • 1,687.14CNY

  • Detail

54802-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-1-benzofuran-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-amino-3-benzofuran-2-carboxamide

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:54802-10-7 SDS

54802-10-7Relevant articles and documents

A benzofuran-β-Alaninamide based "turn-on" fluorescent chemosensor for selective recognition of Fe3+ ions

Madhu,Sivakumar,Sribalan, Rajendran

, p. 14426 - 14434 (2019/09/30)

A benzofuran-β-Alaninamide based chemosensor, 3-(3-((4-methylbenzyl)amino)propanamido)benzofuran-2-carboxamide (BAA), was designed and synthesized for selective detection of Fe3+ ions. The binding ability of BAA towards Fe3+ in DMSO/

The design, synthesis, and biological evaluation of PIM kinase inhibitors

Tsuhako, Amy Lew,Brown, David S.,Koltun, Elena S.,Aay, Naing,Arcalas, Arlyn,Chan, Vicky,Du, Hongwang,Engst, Stefan,Franzini, Maurizio,Galan, Adam,Huang, Ping,Johnston, Stuart,Kane, Brian,Kim, Moon H.,Douglas Laird,Lin, Rui,Mock, Lillian,Ngan, Iris,Pack, Michael,Stott, Gordon,Stout, Thomas J.,Yu, Peiwen,Zaharia, Cristiana,Zhang, Wentao,Zhou, Peiwen,Nuss, John M.,Kearney, Patrick C.,Xu, Wei

scheme or table, p. 3732 - 3738 (2012/07/17)

A series of substituted benzofuropyrimidinones with pan-PIM activities and excellent selectivity against a panel of diverse kinases is described. Initial exploration identified aryl benzofuropyrimidinones that were potent, but had cell permeability limitation. Using X-ray crystal structures of the bound PIM-1 complexes with 3, 5m, and 6d, we were able to guide the SAR and identify the alkyl benzofuropyrimidinone (6l) with good PIM potencies, permeability, and oral exposure.

Syntheses of 3-acetoacetylaminobenzo[b]furan derivatives having cysteinyl leukotriene 2 receptor antagonistic activity

Ando, Kumiko,Tsuji, Eriko,Ando, Yuko,Kuwata, Noriko,Kunitomo, Jun-Ichi,Yamashita, Masayuki,Ohta, Shunsaku,Kohno, Shigekatsu,Ohishi, Yoshitaka

, p. 625 - 635 (2007/10/03)

Novel 3-acetoacetylaminobenzo[b]furan derivatives having a modified triene system at the 3-position were synthesized starting with 3-aminobenzo[b]furans. The enol isomers, 3-[(3-hydroxybul-2-enonyl)amino]benzo[b]furans (1), of the 3-acetoacetylaminobenzo[b]furans were obtained as stable isomers owing to formation of a hydrogen bonding between the enol hydroxyl group and the amidocarbonyl group. The planarity of the C-2 substituent through the C-3 side chain suggested the existence of a modified conjugational triene system in the enol compound. Cysteinyl leukotriene 1 and 2 receptor antagonistic activities for these compounds were evaluated. 2-(4-Cyanobenzoyl or ethoxycarbonyl)-3-[(2-cyano-3-hydroxybut-2-enonyl)amino]benzo[e]furans (15g, 15o, 15u) were moderately active.

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