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2H-1-Benzopyran-2-one, 8-methoxy-3-(4-nitrophenyl)-, also known as 8-methoxy-3-(4-nitrophenyl)-2H-chromen-2-one, is a chemical compound with the molecular formula C16H11NO5. It is a derivative of the benzopyran-2-one class, characterized by the presence of a benzene ring fused to a pyran ring, with a carbonyl group at position 2. This specific compound features a methoxy group at position 8 and a 4-nitrophenyl group at position 3. It is an organic compound with potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and functional groups.

1729-03-9

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1729-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1729-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1729-03:
(6*1)+(5*7)+(4*2)+(3*9)+(2*0)+(1*3)=79
79 % 10 = 9
So 1729-03-9 is a valid CAS Registry Number.

1729-03-9SDS

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 8-methoxy-3-(4-nitrophenyl)-2H-chromen-2-one

1.2 Other means of identification

Product number -
Other names 8-methoxy-3-(4-nitro-phenyl)-chromen-2-one

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:1729-03-9 SDS

1729-03-9Downstream Products

1729-03-9Relevant academic research and scientific papers

Structure-Based Optimization of Coumarin hA3 Adenosine Receptor Antagonists

Matos, Maria Jo?o,Vilar, Santiago,Vazquez-Rodriguez, Saleta,Kachler, Sonja,Klotz, Karl-Norbert,Buccioni, Michela,Delogu, Giovanna,Santana, Lourdes,Uriarte, Eugenio,Borges, Fernanda

, p. 2577 - 2587 (2019/12/25)

Adenosine receptors participate in many physiological functions. Molecules that may selectively interact with one of the receptors are favorable multifunctional chemical entities to treat or decelerate the evolution of different diseases. 3-Arylcoumarins

Hydrolysis and substitution effects on the optical properties of coumarin derivatives studied by vibrational spectroscopy and DFT calculation

Khemakhem, Sirine,Elleuch, Slim,Ben Azaza, Najla,Ammar, Houcine,Abid, Younes

, p. 65 - 72 (2018/05/28)

A series of coumarin derivatives have been successfully synthesized. All compounds have been characterized by means of IR and Raman vibrational spectroscopic techniques at the solid state level. Optical absorption and photoluminescence measurements were p

Synthesis and Evaluation of Coumarin-Resveratrol Hybrids as 15-Lipoxygenaze Inhibitors

Rahmani-Nezhad, Samira,Khosravani, Leila,Saeedi, Mina,Divsalar, Kouros,Firoozpour, Loghman,Pourshojaei, Yaghoub,Sarrafi, Yaghoub,Nadri, Hamid,Moradi, Alireza,Mahdavi, Mohammad,Shafiee, Abbas,Foroumadi, Alireza

supporting information, p. 751 - 759 (2015/10/29)

A series of coumarin-resveratrol hybrids, 3-arylcoumarin derivatives 3a-u, were synthesized through the intermolecular condensation reaction of various salicylaldehydes and phenylacetic acids in the presence of 1,4-diazabicyclo[2.2.2]octane under solvent-free conditions. All the synthesized compounds were screened for their inhibitory potency against soybean 15-lipoxygenase. Among them, three compounds (3c, 3j, and 3q) showed good enzyme-inhibitory activities. GRAPHICAL ABSTRACT.

Coumarins: Fast Synthesis by Knoevenagel Condensation under Microwave Irradiation

Bogdal, Dariusz

, p. 468 - 469 (2007/10/03)

Condensation of salicyaldehyde or its derivatives with various derivatives of ethyl acetate in the presence of piperidine leads to the synthesis of coumarins by a solvent free reaction under microwave irradiation.

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