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6328-17-2

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6328-17-2 Usage

Appearance

White crystalline solid

Odor

Sweet

Natural Occurrence

Found in plants like tonka beans and sweet clover

Uses

a. Flavoring agent in tobacco and food products
b. Fragrance in perfumes

Medical Applications

Anticoagulant properties, used in treatment of certain medical conditions

Toxicity

High doses can be toxic and may cause liver damage

Regulation

Use of coumarin is regulated in some countries, particularly in food and cosmetic products due to potential health risks

Check Digit Verification of cas no

The CAS Registry Mumber 6328-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6328-17:
(6*6)+(5*3)+(4*2)+(3*8)+(2*1)+(1*7)=92
92 % 10 = 2
So 6328-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H4O4/c10-7-5-3-1-2-4-6(5)8(11)13-9(7)12/h1-4H

6328-17-2SDS

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 isochromene-1,3,4-trione

1.2 Other means of identification

Product number -
Other names phthalonic 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:6328-17-2 SDS

6328-17-2Relevant articles and documents

Ozonolysis of enol ethers. Part 10. Ozonization of enol ethers from 1,2- and 1,3-dicarbonyl compounds: Direct quantitative synthesis of phthalonic acid anhydride

Schank, Kurt,Beck, Horst,Pistorius, Susanne

, p. 2025 - 2049 (2007/10/03)

The results of ozonolyses of enol ethers from 1.2- and 1.3-dicarbonyl compounds presented here strongly indicate that these reactions do not proceed via the established Criegee ozonolysis mechanism for nucleophilic C=C bonds. The quantitative one-step synthesis of phthalonic acid anhydride via ozonolysis of 2-(methoxymethyliden)-1H-inden-1.3(2H)-dione (28a) is described. Furthermore, a revision of the theory of alkene ozonolysis in the presence of tetracyanoethylene (TCNE) is proposed on the basis of a single-electron-transfer (SET) chemistry.

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