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1-Oxa-2-azaspiro[2.4]heptane-4-carboxylic acid, 4-methyl-2-(2-phenylethyl)-, ethyl ester is a complex organic compound with the chemical formula C18H23NO3. It is a derivative of spiro[2.4]heptane, featuring a carboxylic acid group, a methyl group, a phenylethyl group, and an ethyl ester group. 1-Oxa-2-azaspiro[2.4]heptane-4-carboxylic acid, 4-methyl-2-(2-phenylethyl)-, ethyl ester is characterized by its unique spirocycle structure, which consists of a seven-membered ring with one oxygen and one nitrogen atom. The presence of the carboxylic acid group makes it an acidic compound, while the ethyl ester group indicates that it is an ester derivative. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds due to its versatile structure and functional groups.

89241-12-3

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89241-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89241-12-3 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 89241-12:
(7*8)+(6*9)+(5*2)+(4*4)+(3*1)+(2*1)+(1*2)=143
143 % 10 = 3
So 89241-12-3 is a valid CAS Registry Number.

89241-12-3SDS

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-(β-phenethyl)-3,3-(2-carboethoxy-2-methyl) tetramethylene-oxazirane

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-phenethyl-1-oxa-2-aza-spiro[2.4]heptane-4-carboxylic acid ethyl ester

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:89241-12-3 SDS

89241-12-3Relevant 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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