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72498-23-8

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72498-23-8 Usage

General Description

"(6aS)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo[de,g]quinoline 6-oxide" is a chemical compound with a complex molecular structure. It belongs to the class of dibenzylisoquinoline alkaloids and is a potent antioxidant with potential applications in medicine and nutrition. The compound is derived from natural sources and has been found to possess anti-inflammatory and anti-cancer properties. Its unique structure and biological activity make it a subject of interest for research and development in the pharmaceutical and nutraceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 72498-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,9 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72498-23:
(7*7)+(6*2)+(5*4)+(4*9)+(3*8)+(2*2)+(1*3)=148
148 % 10 = 8
So 72498-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H25NO5/c1-22(23)7-6-12-9-18(26-4)21(27-5)20-14-11-17(25-3)16(24-2)10-13(14)8-15(22)19(12)20/h9-11,15H,6-8H2,1-5H3/t15-,22?/m0/s1

72498-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,9,10-tetramethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-ium

1.2 Other means of identification

Product number -
Other names (6aS)-1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 6-oxide

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:72498-23-8 SDS

72498-23-8Relevant articles and documents

A facile method for the synthesis of glaucine and norglaucine from boldine

Huang, Wei-Jan,Chen, Chung-Hsiung,Singh, Om V.,Lee, Su-Lin,Lee, Shoei-Sheng

, p. 3681 - 3686 (2007/10/03)

A large-scale preparation of glaucine was achieved by reacting boldine with trimethylphenylammonium chloride and potassium t-butoxide in high yield. Treatment of glaucine with 30% H202, subsequent with hydrated ferrous sulfate, afforded norglaucine in an overall yield of 40%.

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