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7140-45-6

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7140-45-6 Usage

General Description

2,3-dihydro-1,4-ethanoquinoxaline is a chemical compound with the molecular formula C10H10N2. It is a bicyclic heterocycle that contains two nitrogen atoms in its structure. 2,3-dihydro-1,4-ethanoquinoxaline is commonly used in organic synthesis and medicinal chemistry as a building block for creating various molecules and pharmaceutical drugs. It has also shown potential as a psychoactive drug in research studies. Additionally, 2,3-dihydro-1,4-ethanoquinoxaline is known for its ability to act as a ligand in coordination chemistry, forming complexes with transition metal ions. Its versatile properties and applications make it an important compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 7140-45-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7140-45:
(6*7)+(5*1)+(4*4)+(3*0)+(2*4)+(1*5)=76
76 % 10 = 6
So 7140-45-6 is a valid CAS Registry Number.

7140-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Ethanoquinoxaline, 2,3-dihydro-

1.2 Other means of identification

Product number -
Other names Benzo[b]-1,4-diazabicyclo[2.2.2]octane

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:7140-45-6 SDS

7140-45-6Relevant articles and documents

DIAZABICYCLOALKANES WITH BRIDGEHEAD NITROGEN ATOMS. 26. REACTIONS OF HYDROXYETHYL BENZO-1,4-DIAZABICYCLOOCTENES

Doronina, S. O.,Gall', A. A.,Shishkin, G. V.

, p. 917 - 920 (1992)

By heating 1-(2-hydroxyethyl)benzo-1-azonium-4-azabicyclo-octene halides in anhydrous solvents or via thermolysis, opening of the bicycle occurs with formation of the corresponding N-(2-hydroxyethyl)-N'-(2-haloethyl)-1,2,3,4-tetrahydroquinoxalines.In the presence of base, fission of the hydroxyethyl group principally occurs.

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