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74794-52-8

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74794-52-8 Usage

Chemical class

Benzopyranones

Occurrence

Naturally occurring in many plants as a secondary metabolite

Odor

Distinctive sweet odor

Uses

Perfumes and cosmetic products

Biological activities

Anti-inflammatory, antioxidant, and anticoagulant properties

Toxicity

Toxic effects at high doses and implicated in liver toxicity

Regulation

Use as a food additive has been regulated in some countries

Check Digit Verification of cas no

The CAS Registry Mumber 74794-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74794-52:
(7*7)+(6*4)+(5*7)+(4*9)+(3*4)+(2*5)+(1*2)=168
168 % 10 = 8
So 74794-52-8 is a valid CAS Registry Number.

74794-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-methoxy-4H-isochromene-1,3-dione

1.2 Other means of identification

Product number -
Other names 3-methoxyhomophthalic anhydride

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:74794-52-8 SDS

74794-52-8Relevant articles and documents

SYNTHETIC STUDIES ON NOGALAMYCIN CONGENERS ; SYNTHESES AND ANTITUMOR ACTIVITY OF VARIOUS NOGALAMYCIN CONGENERS

Matsuda, Fuyuhiko,Kawasaki, Motoji,Ohsaki, Masako,Yamada, Kaoru,Terashima, Shiro

, p. 5745 - 5760 (2007/10/02)

Various structural types of nogalamycin congeners and their partial structures, which had been previously synthesized in the course of our synthetic studies on the total syntheses or were originally produced by employing the explored synthetic scheme, were subjected to in vitro cytotoxicity and in vivo antitumor activity assay against P388 murine leukemia.These studies obviously disclosed novel aspects of the structure-activity relationships of nogalamycin congeners.

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