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4-Hydroxy-3-(p-tolyl)-2H-1-benzopyran-2-one, commonly known as umbelliferone, is a naturally occurring compound found in a variety of plants, including carrots, milk thistle, and oranges. It is characterized by its pleasant fragrance and sweet taste, which have historically been utilized in the preparation of perfumes and as a flavoring agent. Umbelliferone also exhibits a range of biological activities, such as antioxidant, anti-inflammatory, and anti-cancer properties, and has been studied for its potential therapeutic applications in treating conditions like diabetes, osteoporosis, and neurodegenerative disorders. Its multifaceted properties and potential health benefits highlight umbelliferone as a compound of significant interest for ongoing research and development in pharmaceuticals and nutraceuticals.

73791-19-2

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73791-19-2 Usage

Uses

Used in Perfumery and Flavoring Industry:
Umbelliferone is used as a fragrance ingredient and flavoring agent in the perfumery and flavoring industry due to its pleasant aroma and sweet taste, enhancing the sensory experience of various products.
Used in Pharmaceutical Applications:
Umbelliferone is utilized as a pharmaceutical compound for its antioxidant, anti-inflammatory, and anti-cancer properties, making it a potential candidate for the development of treatments for a range of diseases.
Used in Nutraceutical Applications:
In the nutraceutical industry, umbelliferone is employed for its potential health benefits, including its role in the prevention and treatment of conditions such as diabetes, osteoporosis, and neurodegenerative disorders, contributing to overall health and well-being.
Used in Therapeutic Research:
Umbelliferone is used as a subject of therapeutic research for its potential applications in treating various diseases, reflecting its diverse range of biological activities and the ongoing interest in exploring its full potential in medical and health-related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 73791-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,9 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73791-19:
(7*7)+(6*3)+(5*7)+(4*9)+(3*1)+(2*1)+(1*9)=152
152 % 10 = 2
So 73791-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O3/c1-10-6-8-11(9-7-10)14-15(17)12-4-2-3-5-13(12)19-16(14)18/h2-9,18H,1H3

73791-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3-(4-methylphenyl)chromen-2-one

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3-p-tolyl-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:73791-19-2 SDS

73791-19-2Downstream Products

73791-19-2Relevant academic research and scientific papers

Antitrypanosomal and antioxidant properties of 4-hydroxycoumarins derivatives

Perez-Cruz, Fernanda,Serra, Silvia,Delogu, Giovanna,Lapier, Michel,Maya, Juan Diego,Olea-Azar, Claudio,Santana, Lourdes,Uriarte, Eugenio

experimental part, p. 5569 - 5573 (2012/09/25)

In the present communication we prepared a series of six 4-hydroxycoumarin derivatives, isosters of quercetin, recognized as an antioxidant natural compound, with the aim of evaluating the antitrypanosomal activity against Trypanosoma cruzi, the parasite

The rhodium carbenoid route to 3-aryl-4-hydroxycoumarins: Synthesis of derrusnin

Goldoni, Luca,Cravotto, Giancarlo,Penoni, Andrea,Tollari, Stefano,Palmisano, Giovanni

, p. 927 - 930 (2007/10/03)

3-Aryl-4-hydroxycoumarins have been obtained in satisfactory yields and selectivity through a Rh(II)-mediated arylation of diazocoumarin. The utility of this approach is demonstrated by synthesis of the natural product derrusnin.

Application of Aryllead(IV) Derivatives to the Preparation of 3-Aryl-4-hydroxy-1-benzopyran-2-ones

Barton, Derek H. R.,Donnelly, Dervilla M. X.,Finet, Jean-Pierre,Guiry, Patrick J.

, p. 1365 - 1376 (2007/10/02)

Aryllead triacetates are chemoselective and regioselective reagents for the preparation of 3-aryl-4-hydroxy-1-benzopyran-2-ones in good to excellent yields by C-3 arylation of the preformed 4-hydroxy-1-benzopyran-2-one ring.This approach was applied to th

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