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3-Oxa-6-azabicyclo[3.1.0]hexane is a heterocyclic organic compound with the molecular formula C5H9NO. It features a bicyclic structure, where one ring is a three-membered oxirane (epoxy) ring and the other is a three-membered aziridine ring. The compound is characterized by the presence of one oxygen atom and one nitrogen atom in the bicyclic structure, with the nitrogen atom being part of the aziridine ring. This unique structure endows 3-oxa-6-azabicyclo[3.1.0]hexane with specific chemical properties and reactivity, making it a potentially useful building block in the synthesis of various pharmaceuticals and other organic compounds.

5834-36-6

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5834-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5834-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5834-36:
(6*5)+(5*8)+(4*3)+(3*4)+(2*3)+(1*6)=106
106 % 10 = 6
So 5834-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO/c1-3-4(5-3)2-6-1/h3-5H,1-2H2

5834-36-6SDS

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 3-oxa-6-azabicyclo[3.1.0]hexane

1.2 Other means of identification

Product number -
Other names 3-Oxa-6-aza-bicyclo<3.1.0>hexan

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 -
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More Details:5834-36-6 SDS

5834-36-6Downstream Products

5834-36-6Relevant academic research and scientific papers

Enantioselective ring-opening of aziridines

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Page/Page column 15-16, (2009/02/11)

A process for the preparation of a nucleophilic addition product of an aziridine and a nucleophile, the process comprising treating the arizidine with the nucleophile in the presence of a biaryl phosphoric acid catalyst

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