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N1,N1-Dimethyl-N2-[4-(trifluoromethyl)phenyl]formamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29366-21-0

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29366-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29366-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,6 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29366-21:
(7*2)+(6*9)+(5*3)+(4*6)+(3*6)+(2*2)+(1*1)=130
130 % 10 = 0
So 29366-21-0 is a valid CAS Registry Number.

29366-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-N'-[4-(trifluoromethyl)phenyl]methanimidamide

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-N'-(p-trifluormethylphenyl)-formamidin

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:29366-21-0 SDS

29366-21-0Downstream Products

29366-21-0Relevant academic research and scientific papers

Cyclization of C-phosphorylated (PIII) arylformamidines to 3H-1,3-benzazaphospholes

Marchenko, Anatolyi,Koidan, Heorgii,Hurieva, Anastasiya,Merkulov, Anatolyi,Pinchuk, Aleksandr,Yurchenko, Aleksandr,Rozhenko, Alexander B.,Jones, Peter G.,Th?nnessen, Holger,Kostyuk, Aleksandr

experimental part, p. 7748 - 7758 (2011/10/17)

A synthesis of 3H-1,3-benzazaphospholes starting from C-phosphorylated P(III) arylformamidines has been developed. Electron-donating substituents were found to enhance markedly the rate of the cyclization, with substituents at the meta position having the greatest effect. A plausible mechanism of the cyclization was proposed based on DFT calculations.

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