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Diaziridine, 3,3-difluoro-1-(trifluoromethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91523-64-7

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91523-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91523-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91523-64:
(7*9)+(6*1)+(5*5)+(4*2)+(3*3)+(2*6)+(1*4)=127
127 % 10 = 7
So 91523-64-7 is a valid CAS Registry Number.

91523-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-Difluoro-1-trifluoromethyl-diaziridine

1.2 Other means of identification

Product number -
Other names -

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:91523-64-7 SDS

91523-64-7Downstream Products

91523-64-7Relevant academic research and scientific papers

Some Novel Reactions of N-Chlorodifluoromethanimine

Zheng, Yuan Y.,Bauknight, Charles W.,DesMarteau, Darryl D.

, p. 3590 - 3595 (1984)

Some reactions of N-chlorodifluoromethanimine, CF2=NCl, have been studied and are compared to related reactions of perfluoromethanimine, CF2=NF.Fluoride promoted reactions of CF2=NCl result in evidence for the CF3NCl- anion, which is thermally less stable and less reactive than CF3NF-.Oxidation of CF3NCl-, formed in situ by reaction of CF2=NCl with KF or CsF, with Cl2 forms CF3NCl2.With Br2, CF3NBrCl is formed along with CF3NBr2.The latter arises from a novel fluoride-catalyzed conversion of CF3NBrCl to CF3NBr2 by Br2, and the same products can be obtained starting with CF3NCl2, Br2, and MF.Extension of this reaction to C2F5NCl2 and C3F7NCl2 is also discussed.Addition of XOSO2F (X=Cl, Br) to CF2=NCl forms the novel diazene FSO2OCF2N=NCF2OSO2F, presumably via the intermediate FSO2OCF2NClX addition products.Competitive reaction of CF2=NF and CF2=NCl with fluoride ion results in the preferential formation of CF3NF-.Nucleophilic attack of the latter on CF2=NCl forms the novel diaziridine , which can be reduced by Hg in trifluoroacetic acid to .The mechanism for the formation of the diaziridines is discussed.

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