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1-methyl-2-(4-chlorophenyl)aziridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66295-99-6

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66295-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66295-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,9 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66295-99:
(7*6)+(6*6)+(5*2)+(4*9)+(3*5)+(2*9)+(1*9)=166
166 % 10 = 6
So 66295-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClN/c1-11-6-9(11)7-2-4-8(10)5-3-7/h2-5,9H,6H2,1H3

66295-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-1-methylaziridine

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-para-chlorophenylaziridine

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:66295-99-6 SDS

66295-99-6Relevant academic research and scientific papers

Diethylammonium iodide as catalyst for the metal-free synthesis of 5-aryl-2-oxazolidinones from aziridines and carbon dioxide

Bresciani, Giulio,Bortoluzzi, Marco,Pampaloni, Guido,Marchetti, Fabio

, p. 4152 - 4161 (2021/05/19)

The catalytic potential of ammonium halide salts was explored in the coupling reaction of a model aziridine with carbon dioxide, highlighting the superior activity of [NH2Et2]I. Then, working at room temperature, atmospheric CO2 pressure and in the absenc

METHOD FOR SYNTHESIZING AN N-UNSUBSTITUTED OR N-SUBSTITUTED AZIRIDINE

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Page/Page column 5, (2010/08/07)

Process for preparing an N-unsubstituted or N-substituted aziridine of the formula which comprises reacting an olefin of the formula I where R1 to R5 are each, independently of one another, hydrogen, a linear or branched alkyl radica

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