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4H-1-Benzopyran-4-one, 2-(2-furanyl)-2,3-dihydro-, also known as Coumarin, is a naturally occurring organic compound belonging to the class of benzopyrones. It is characterized by a benzene ring fused to a pyran ring, with a carbonyl group at position 4 and a furan ring attached at position 2. Coumarin is widely found in plants, particularly in the tonka bean, and is known for its pleasant aroma. It is used in various applications, including as a flavoring agent in food and beverages, a fragrance in perfumes, and a chemical intermediate in the synthesis of other compounds. Additionally, it has been studied for its potential medicinal properties, such as anticoagulant and anti-inflammatory effects.

3327-26-2

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3327-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3327-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3327-26:
(6*3)+(5*3)+(4*2)+(3*7)+(2*2)+(1*6)=72
72 % 10 = 2
So 3327-26-2 is a valid CAS Registry Number.

3327-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(furan-2-yl)-2,3-dihydrochromen-4-one

1.2 Other means of identification

Product number -
Other names 2-furan-2-yl-chroman-4-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 -
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More Details:3327-26-2 SDS

3327-26-2Downstream Products

3327-26-2Relevant academic research and scientific papers

New synthesis of flavanones catalyzed by L-proline

Chandrasekhar,Vijeender,Venkatram Reddy

, p. 6991 - 6993 (2005)

L-Proline is utilized as an efficient organocatalyst for the synthesis of substituted flavanones and chalcones in good yields. The efficiency of the catalyst was proved with a variety of substrates ranging from electron-deficient to electron-rich aryl aldehydes and 2-hydroxyacetophenones.

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