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107408-81-1

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  • 2,3,5,6-1H,4H-TETRAHYDRO-8-METHOXYCARBONYL-QUINOLIZINO- (9,9A,1-GH)COUMARIN

    Cas No: 107408-81-1

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107408-81-1 Usage

Chemical Class

Coumarins

Ring System

Tetrahydroquinoline fused to a coumarin ring

Substituent

Methoxycarbonyl group at the 8th position

Pharmacological Activities

Anti-inflammatory, anticoagulant, and anticancer properties

Potential Applications

Therapeutic uses, medicinal chemistry research

Suitability for Study

Complex structure, organic chemistry research

Check Digit Verification of cas no

The CAS Registry Mumber 107408-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,0 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107408-81:
(8*1)+(7*0)+(6*7)+(5*4)+(4*0)+(3*8)+(2*8)+(1*1)=111
111 % 10 = 1
So 107408-81-1 is a valid CAS Registry Number.

107408-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name coumarin 343 methyl ester

1.2 Other means of identification

Product number -
Other names -

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:107408-81-1 SDS

107408-81-1Downstream Products

107408-81-1Relevant articles and documents

Chemiluminescence of Organic Peroxides: Intramolecular Electron-Exchange Luminescence from a Secondary Perester

Gompel, Joseph Van,Schuster, Gary B.

, p. 1465 - 1468 (1987)

The reaction of an aminocoumarincarboxylic acid chloride (Coumarin 343) with 1-phenethyl hydroperoxide results in light emission that is easily detected with the unaided eye.This reaction proceeds through a secondary perester intermediate.Intramolecular electron exchange, modeled after the analogous process in the bioluminescence of the firefly, is proposed as the mechanism for light generation.Attempts to carry out this reaction under conditions where the coumarin acid is recycled were not successful.

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