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1-Oxa-2-azaspiro[2.4]heptane, 2-[2-(3,4-dimethoxyphenyl)ethyl]- is a complex organic compound with a unique molecular structure. It is characterized by a spiro ring system, which consists of a seven-membered ring with one oxygen atom and one nitrogen atom. The compound features a 3,4-dimethoxyphenyl group attached to an ethyl chain, which is further connected to the spiro ring system. This specific arrangement of atoms and functional groups gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

89241-16-7

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89241-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89241-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,4 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89241-16:
(7*8)+(6*9)+(5*2)+(4*4)+(3*1)+(2*1)+(1*6)=147
147 % 10 = 7
So 89241-16-7 is a valid CAS Registry Number.

89241-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(3,4-dimethoxyphenyl)ethyl]-1-oxa-2-azaspiro[2.4]heptane

1.2 Other means of identification

Product number -
Other names 1-Oxa-2-azaspiro[2.4]heptane,2-[2-(3,4-dimethoxyphenyl)ethyl]

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:89241-16-7 SDS

89241-16-7Relevant academic research and scientific papers

THE PHOTOCHEMICAL OR THERMAL REARRANGEMENT OF OXAZIRANES AS A METHOD IN ALKALOID SYNTHESIS

Kuehne, Martin E.,Parsons, W. H.

, p. 3763 - 3766 (2007/10/02)

The conversion of cyclic ketones to β-arylethyl amine derived imines, their oxidation to oxaziranes and subsequent photochemical rearrangement to N-(β-arylethyl) lactams was probed as a potential method for alkaloid syntheses.

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