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13229-92-0

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13229-92-0 Usage

General Description

3-CYANO-7-METHOXYCOUMARIN is a chemical compound that belongs to the coumarin family. It is a derivative of coumarin and is characterized by a cyano group at the 3-position and a methoxy group at the 7-position of the coumarin ring. 3-CYANO-7-METHOXYCOUMARIN is known for its fluorescent properties and is often used as a fluorescent probe in biological and chemical research. Additionally, it has been studied for its potential pharmacological activities, including its antioxidant, anti-inflammatory, and antimicrobial properties. 3-CYANO-7-METHOXYCOUMARIN has a wide range of potential applications in various fields, making it a compound of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 13229-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13229-92:
(7*1)+(6*3)+(5*2)+(4*2)+(3*9)+(2*9)+(1*2)=90
90 % 10 = 0
So 13229-92-0 is a valid CAS Registry Number.

13229-92-0 Well-known Company Product Price

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  • Sigma

  • (UC454)  3-Cyano-7-methoxycoumarin  

  • 13229-92-0

  • UC454-5MG

  • 2,277.99CNY

  • Detail
  • Sigma

  • (UC454)  3-Cyano-7-methoxycoumarin  

  • 13229-92-0

  • UC454-10MG

  • 4,188.60CNY

  • Detail

13229-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-2-oxochromene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 7-Methoxy-2-oxo-2H-chromen-3-carbonitril

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:13229-92-0 SDS

13229-92-0Relevant articles and documents

Organo Photoinduced Decarboxylative Alkylation of Coumarins with N-(Acyloxy)phthalimide

Tripathi, Krishna N.,Belal, Md.,Singh, Ravi P.

, p. 1193 - 1201 (2020)

A metal-free and mild, photoinduced decarboxylative 4-position alkylation of coumarins has been reported. Photoinduced single electron transfer has been initiated by utilizing the visible-light absorptivity of Eosin Y for a reductive generation of alkyl r

Sonochemistry as a General Procedure for the Synthesis of Coumarins, Including Multigram Synthesis

Da Silveira Pinto, Ligia S.,De Souza, Marcus V. N.

, p. 2677 - 2682 (2017)

This study describes a general procedure for the synthesis of different coumarins via sonochemistry using active methylene compounds and 2-hydroxybenzaldehydes or resorcinol. The application of sonochemistry for the synthesis of these compounds was also very effective on a multigram scale with a higher yield, higher amount of crystalline compound, and shorter reaction time compared with the compounds obtained using the classical procedures.

ZrCl4/[bmim]BF4-catalyzed condensation of salicylaldehydes and malononitrile: Single-step synthesis of 3-cyanocoumarin derivatives

Valizadeh, Hassan,Mahmoodian, Manzar,Gholipour, Hamid

, p. 799 - 802 (2011)

Figure represented. A versatile and efficient single-step route to 3-cyanocoumarins via Knoevenagel condensation of salicylaldehydes and malononitrile using ZrCl4 as the catalyst (15 mol %) in ionic liquid 1-(n-butyl)-3-methylimidazolium tetrafluoroborate as reaction medium and catalyst is described. The novel procedure features single step, short reaction time, good yields, and simple workup.

One-Pot Green Synthesis of 2-Oxo-2H-chromene-3-carbonitriles Using Dual-Frequency Ultrasonication

Aruna,Kumar, S.,Sharma, S. P.,Vashisht, N.

, p. 1508 - 1512 (2021/10/26)

Abstract: A green synthesis of 2-oxo-2H-chromene-3-carbonitriles has been carried out in one step by reacting 2-hydroxybenzaldehydes or 2-hydroxyacetophenones with ethyl cyanoacetate under dual-frequency ultrasonica-tion (ultrasonic bath of 40 KHz and probe of 20 KHz). The compounds were obtained in very high yield, and their structures were confirmed by IR and NMR data.

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