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151731-50-9

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151731-50-9 Usage

General Description

2,2-Dimethyl-8-prenyl-2H-chromene-6-carboxylic acid is a chemical compound with potential pharmaceutical and therapeutic applications. It belongs to the class of organic compounds known as flavonoids, which are known for their antioxidant and anti-inflammatory properties. This particular compound is derived from plants and has shown promise in various studies for its potential anti-cancer, anti-diabetic, and neuroprotective effects. Its unique chemical structure and biological activities make it a valuable candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 151731-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,7,3 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151731-50:
(8*1)+(7*5)+(6*1)+(5*7)+(4*3)+(3*1)+(2*5)+(1*0)=109
109 % 10 = 9
So 151731-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O3/c1-11(2)5-6-12-9-14(16(18)19)10-13-7-8-17(3,4)20-15(12)13/h5,7-10H,6H2,1-4H3,(H,18,19)

151731-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-8-(3-methylbut-2-enyl)chromene-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-8-prenylchromene 6-carboxylic acid

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:151731-50-9 SDS

151731-50-9Downstream Products

151731-50-9Relevant articles and documents

Antifungal activity of chemical constituents from piper pesaresanum C. DC. and derivatives against phytopathogen fungi of cocoa

Chitiva-Chitiva, Luis C.,Cuca-Suárez, Luis E.,Ladino-Vargas, Cristóbal,Pati?o-Ladino, Oscar J.,Prieto-Rodríguez, Juliet A.

, (2021)

In this study, the antifungal potential of chemical constituents from Piper pesaresanum and some synthesized derivatives was determined against three phytopathogenic fungi associated with the cocoa crop. The methodology included the phytochemical study on the aerial part of P. pesaresanum, the synthesis of some derivatives and the evaluation of the antifungal activity against the fungi Moniliophthora roreri, Fusarium solani and Phytophthora sp. The chemical study allowed the isolation of three benzoic acid derivatives (1–3), one dihydrochalcone (4) and a mixture of sterols (5–7). Seven derivatives (8–14) were synthesized from the main constituents, of which compounds 9, 10, 12 and 14 are reported for the first time. Benzoic acid derivatives showed strong antifungal activity against M. roreri, of which 11 (3.0 ± 0.8 μM) was the most active compound with an IC50 lower compared with positive control Mancozeb (4.9 ± 0.4 μM). Dihydrochalcones and acid derivatives were active against F. solani and Phytophthora sp., of which 3 (32.5 ± 3.3 μM) and 4 (26.7 ± 5.3 μM) were the most active compounds, respectively. The preliminary structure–activity relationship allowed us to establish that prenylated chains and the carboxyl group are important in the antifungal activity of benzoic acid derivatives. Likewise, a positive influence of the carbonyl group on the antifungal activity for dihydrochalcones was deduced.

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