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20988-30-1

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20988-30-1 Usage

General Description

α-[4-(3,4-Dihydroxyphenyl)-3-hydroxy-5-oxofuran-2(5H)-ylidene]-3,4-dihydroxybenzeneacetic acid is a chemical compound that contains a furan ring fused to a benzene ring. It also has two hydroxyl groups attached to the furan ring and two hydroxyl groups attached to the benzene ring, as well as a carboxylic acid group attached to the benzene ring. α-[4-(3,4-Dihydroxyphenyl)-3-hydroxy-5-oxofuran-2(5H)-ylidene]-3,4-dihydroxybenzeneacetic acid is known for its antioxidant and anti-inflammatory properties, making it potentially useful for treating conditions such as arthritis, cardiovascular disease, and cancer. Additionally, its unique structure and properties make it a valuable compound for further research and potential drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 20988-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20988-30:
(7*2)+(6*0)+(5*9)+(4*8)+(3*8)+(2*3)+(1*0)=121
121 % 10 = 1
So 20988-30-1 is a valid CAS Registry Number.

20988-30-1SDS

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 variegatic acid

1.2 Other means of identification

Product number -
Other names Variegatsaeure

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:20988-30-1 SDS

20988-30-1Downstream Products

20988-30-1Relevant articles and documents

Synthesis of natural pulvinic acids based on a '[3+2] cyclization-Suzuki cross-coupling' strategy

Ahmed, Zafar,Langer, Peter

, p. 2055 - 2063 (2007/10/03)

A number of pulvinic acid natural products were prepared based on Suzuki cross coupling reactions of α-hydroxy-γ-alkylidenebutenolides which are readily available by cyclization of 1,3-bis-silyl enol ethers with oxalyl chloride. The formal total synthesis

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