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2543-95-5

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2543-95-5 Usage

General Description

(S)-4-Methoxydalbergione is a natural chemical compound found in several plants, including the potato. It belongs to the class of compounds known as quinones, which are redox-active molecules involved in various cellular processes. (S)-4-METHOXYDALBERGIONE has been studied for its potential antioxidant and anticancer properties, as well as its ability to inhibit the activity of certain enzymes. It is also being investigated for its potential to be used in the production of colored dyes and as a chemical intermediate in organic synthesis. Its structure and properties make it a promising molecule for further research in the fields of medicine, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 2543-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2543-95:
(6*2)+(5*5)+(4*4)+(3*3)+(2*9)+(1*5)=85
85 % 10 = 5
So 2543-95-5 is a valid CAS Registry Number.

2543-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(-)-4-methoxydalbergione

1.2 Other means of identification

Product number -
Other names 2-Methoxy-5-((S)-1-phenyl-allyl)-[1,4]benzoquinone

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:2543-95-5 SDS

2543-95-5Downstream Products

2543-95-5Relevant articles and documents

Enantioselective addition of boronates to o -quinone methides catalyzed by chiral biphenols

Luan, Yi,Schaus, Scott E.

, p. 19965 - 19968 (2013/02/22)

Chiral biphenols were found to catalyze the enantioselective asymmetric addition of aryl- or alkenylboronates to o-quinone methides. Substituted 2-styryl phenols were obtained in good yields (up to 95%) with high enantiomeric ratios (up to 98:2) in the pr

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