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Aziridine, 1,1-carbonylbis[2-methyl- (7CI,8CI,9CI)] is a chemical compound with the molecular formula C6H11NO2. It is a cyclic amine derivative, specifically a 2-methylaziridine with a carbonyl group bridging two of its carbon atoms. Aziridine, 1,1-carbonylbis[2-methyl- (7CI,8CI,9CI) is known for its potential applications in organic synthesis and as a building block for more complex molecules. It is important to note that aziridine derivatives can be reactive and may have specific handling and safety requirements due to their potential reactivity and toxicity.

7259-82-7

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7259-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7259-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7259-82:
(6*7)+(5*2)+(4*5)+(3*9)+(2*8)+(1*2)=117
117 % 10 = 7
So 7259-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O/c1-5-3-8(5)7(10)9-4-6(9)2/h5-6H,3-4H2,1-2H3

7259-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-methylaziridin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names N,N,N',N'-di(propylene)urea

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:7259-82-7 SDS

7259-82-7Downstream Products

7259-82-7Relevant academic research and scientific papers

Process for the production of high energy materials

-

, (2008/06/13)

A process for the production of a high energy nitrate ester involves reacting, in an inert organic solvent, a heterocyclic compound, selected from oxiranes, oxetanes, N-substituted aziridines and N-substituted azetidines, with either N2 O4 or N2 O5, and when the compound is reacted with N2 O4, oxidizing the O- or N-nitrate substituents or substituent in the product to O- or N-nitrate substituent or substituents. The remaining ring carbon atoms on the heterocyclic compound may be substituted or unsubstituted. Preferred substituent groups for the C and/or N ring atoms on the compound include alkyl, cyanoalkyl, haloalkyl, nitroalkyl, and substituted aryl. Several novel nitrate ester are also provided, including nitrated derivatives of polybutadiene, in which between 1% and 25% of the carbon atoms in the polymer are substituted by vicinal nitrate ester (--ONO2) groups.

ACTION DE CF3OF SUR DES AZIRIDINES N-NON SUBSTITUEES

Seguin, M.,Adenis, J. C.,Michaud, C.,Basselier, J. J.

, p. 37 - 48 (2007/10/02)

Aziridines I react with trifluoromethyl hypofluorite at -40 deg C to produce mixtures of 1-(aziridine)carbonyl fluoride II and 1-fluoroaziridine III, the proportions of which depend on steric effects.Several compounds II react with starting materials to g

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