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124858-37-3

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124858-37-3 Usage

General Description

5-Dehydroxyparatocarpin K is a chemical compound that belongs to the flavonoid family and is commonly found in natural products such as plants and fruits. 5-Dehydroxyparatocarpin K has been found to have various biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties. It has also been studied for its potential in treating cancer and obesity. Additionally, 5-Dehydroxyparatocarpin K has shown promise as a potential therapeutic agent for various diseases and conditions. Its diverse range of biological activities make it a valuable compound for further research and potential development of new pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 124858-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,8,5 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124858-37:
(8*1)+(7*2)+(6*4)+(5*8)+(4*5)+(3*8)+(2*3)+(1*7)=143
143 % 10 = 3
So 124858-37-3 is a valid CAS Registry Number.

124858-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Dehydroxyparatocarpin K

1.2 Other means of identification

Product number -
Other names -

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:124858-37-3 SDS

124858-37-3Downstream Products

124858-37-3Relevant articles and documents

New Syntheses of 4',7-Dihydroxy-6,8-di-C-prenylflavanone, Bavachin, Isobavachin and Related Compounds

Krishnamurti, M.,Parthasarathi, J.

, p. 247 - 248 (2007/10/02)

The titel compounds have been synthesised by nuclear prenylation of 4',7-dihydroxyflavanone(liquiritigenin, III), Cyclodehydrogenation of bavachin and isobavachin with DDQ yields the chromenoflavanones (VIII) and (X) respectively which on dehydrogenation

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