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1H-imidazole, 4,5-dihydro-2-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2794-20-9

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2794-20-9 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 3958, 1962 DOI: 10.1021/jo01058a048

Check Digit Verification of cas no

The CAS Registry Mumber 2794-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2794-20:
(6*2)+(5*7)+(4*9)+(3*4)+(2*2)+(1*0)=99
99 % 10 = 9
So 2794-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H5F3N2/c5-4(6,7)3-8-1-2-9-3/h1-2H2,(H,8,9)

2794-20-9SDS

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 2-(trifluoromethyl)-4,5-dihydro-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-trifluoromethyl-4,5-dihydro-1H-imidazole

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:2794-20-9 SDS

2794-20-9Downstream Products

2794-20-9Relevant academic research and scientific papers

Synthesis of 1,1,1-trifluorobut-3-yn-2-ones and their reactions with N-nucleophiles

Muzalevskiy, Vasiliy M.,Iskandarov, Anton A.,Nenajdenko, Valentine G.

, p. 342 - 344 (2015/02/19)

Bromination of 4-aryl-1,1,1-trifluorobut-3-yn-2-ones gives 4-aryl-3,4-dibromo-1,1,1-trifluorobut-3-en-2-ones whose reactivity towards N-nucleophiles (hydrazine and ethylenediamine) was investigated.

REACTIONS OF TRIVALENT PHOSPHORUS COMPOUNDS WITH AZIDES CONTAINING A MOBILE H-ATOM. A CONCEPTION OF PHOSPHAZO-COMPOUND SPIROCYCLIZATION MECHANISM

Gololobov, Yu G.,Gusar, N. I.,Chaus, M. P.

, p. 793 - 800 (2007/10/02)

Investigation of the reactions of α-azidocarboxylic acids, N-(2-azidoethyl)amides and N-(2-azidoethyl)amines with trivalent P compounds shows that the intramolecular cyclization to spirophosphoranes of the intermediate phosphazo-compounds is typical of the azides of the first and third types but not of the second type.It is concluded that such cyclization is possible only where the functional group of the starting azides contains either a sufficiently mobile hydrogen atom or a highly nucleophilic proton-containing group.A new general process for producing imidazolines and oxazolines has been developed.

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