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24604-97-5

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24604-97-5 Usage

Description

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)-, also known as (R)-Hesperetin, is a stereoisomer of (S)-Hesperetin and is the aglucon of Hesperidin, a flavanone found in citrus fruits. It is a naturally occurring compound with a unique chemical structure that has attracted attention for its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)is used as a pharmaceutical compound for its potential therapeutic properties. The compound has been studied for its antioxidant, anti-inflammatory, and anticancer activities, making it a promising candidate for the development of new drugs targeting various diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)is used as a natural ingredient in dietary supplements and functional foods due to its health-promoting properties. Its antioxidant and anti-inflammatory effects contribute to the overall well-being and may help in the prevention of chronic diseases.
Used in Cosmetic Industry:
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)is used as an active ingredient in the cosmetic industry for its potential benefits in skincare products. Its antioxidant properties may help protect the skin from environmental stressors, while its anti-inflammatory effects may soothe and calm irritated skin.
Used in Food and Beverage Industry:
In the food and beverage industry, 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)is used as a natural additive to enhance the flavor, color, and shelf life of various products. Its antioxidant properties may also help in preserving the freshness and quality of the products.
Used in Agricultural Industry:
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (2R)can be used in the agricultural industry as a natural pesticide or growth promoter due to its potential bioactive properties. It may help in protecting crops from pests and diseases, as well as promoting healthy growth and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 24604-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24604-97:
(7*2)+(6*4)+(5*6)+(4*0)+(3*4)+(2*9)+(1*7)=105
105 % 10 = 5
So 24604-97-5 is a valid CAS Registry Number.

24604-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(R)-hesperetin

1.2 Other means of identification

Product number -
Other names (R)-4'-methoxy-3',5,7-trihydroxyflavanone

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:24604-97-5 SDS

24604-97-5Downstream Products

24604-97-5Relevant articles and documents

Functionalities tuned enantioselectivity of phenylcarbamate cyclodextrin clicked chiral stationary phases in HPLC

Tang, Jian,Lin, Yuzhou,Yang, Bo,Zhou, Jie,Tang, Weihua

, p. 566 - 573 (2017/08/26)

The mixed chloro- and methyl- functionalities can greatly modulate the enantioselectivities of phenylcarbamate cyclodextrin (CD) clicked chiral stationary phases (CSPs). A comparison study is herein reported for per(4-chloro-3-methyl)phenylcarbamate and per(2-chloro-5-methyl)phenylcarbamate β-CD clicked CSPs (i.e., CCC4M3-CSP and CCC2M5-CSP). The enantioselectivity dependence on column temperature was studied in both normal-phase and reversed-phase mode high performance liquid chromatography (HPLC). The thermodynamic study revealed that the stronger intermolecular interactions can be formed between CCC4M3-CSP and chiral solutes to drive the chiral separation. The higher enantioselectivities of CCC4M3-CSP were further demonstrated with the enantioseparation of 17 model racemates in HPLC.

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