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2-AMINO-4-ETHYL-5-OXO-4H,5H-PYRANO[3,2-C]CHROMENE-3-CARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

499785-45-4

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499785-45-4 Usage

Family

Pyrano[3,2-c]chromene derivatives

Structural Features

Heterocyclic compound
Contains a pyran ring fused to a chromene ring
Functional Groups:
Amino group
Ethyl group
Carbonyl group
Carbonitrile group

Biological Activities

Antitumor
Antiviral
Antimicrobial

Potential Applications

Medicinal chemistry

Significance

Unique structural features
Diverse pharmacological activities

Research Potential

Interesting chemical for further research
Potential for drug development

Check Digit Verification of cas no

The CAS Registry Mumber 499785-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,8 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 499785-45:
(8*4)+(7*9)+(6*9)+(5*7)+(4*8)+(3*5)+(2*4)+(1*5)=244
244 % 10 = 4
So 499785-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2O3/c1-2-8-10(7-16)14(17)20-13-9-5-3-4-6-11(9)19-15(18)12(8)13/h3-6,8H,2,17H2,1H3

499785-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-ethyl-5-oxo-4H-pyrano[3,2-c]chromene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-amino-4-ethyl-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile

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:499785-45-4 SDS

499785-45-4Downstream Products

499785-45-4Relevant academic research and scientific papers

Another application of (NH4)42[MoVI 72MoV 60O372(CH3COO)30(H2O)72] as a highly efficient recyclable catalyst for the synthesis of dihy

Rohaniyan, Marziyeh,Davoodnia, Abolghasem,Nakhaei, Ahmad

, p. 626 - 629 (2016/07/19)

In continuation of our previous works on the application of (NH4)42[MoVI 72MoV 60O372(CH3COO)30(H2O)72], a Keplerate-type giant-ball n

Design, synthesis, docking study and biological evaluation of some novel tetrahydrochromeno [3′,4′:5,6]pyrano[2,3-b]quinolin-6(7H)-one derivatives against acetyl- and butyrylcholinesterase

Khoobi, Mehdi,Alipour, Masoumeh,Moradi, Alireza,Sakhteman, Amirhossein,Nadri, Hamid,Razavi, Seyyede Faeze,Ghandi, Mehdi,Foroumadi, Alireza,Shafiee, Abbas

, p. 291 - 300 (2013/10/01)

Novel hybrid derivatives of two known scaffolds; tetrahydroaminoquinoline and coumarin were synthesized and evaluated for both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) activities. By means of an efficient nanocatalyst, the reaction time for the syntheses of the target compounds was reduced. Subsequently, Ellman's modified method was used to evaluate the enzyme inhibitory activity of the synthesized structures. It was observed that most hybrid structures were moderate to potent inhibitors of AChE compared to Tacrine as the reference drug among which 7f with 4-fluorophenyl substituent was the most active compound (IC50 = 5 nM).

Mono- and bis-2-amino-4h-pyrans: Alum catalyzed three - or pseudo five-component reaction of 4-hydroxycoumarin, malononitrile and aldehydes

Karimi, Ali Reza,Eslami, Cyrus

, p. 150 - 154 (2013/01/10)

An efficient method for the three- Or pseudo five-component synthesis of mono- and bis-2-amino-4H-pyrans in excellent yields using Alum (KAl(SO 4)2.12H2O) as recyclable catalyst is described. The present methodology offers

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