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1H-Imidazole, 5-fluoro-2-phenyl-4-(trifluoromethyl)-1-(2,4,6-trimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70276-87-8

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70276-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70276-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,7 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70276-87:
(7*7)+(6*0)+(5*2)+(4*7)+(3*6)+(2*8)+(1*7)=128
128 % 10 = 8
So 70276-87-8 is a valid CAS Registry Number.

70276-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4,6-Trimethylphenyl)-5-fluor-2-phenyl-4-(trifluormethyl)imidazol

1.2 Other means of identification

Product number -
Other names 5-Fluor-2-phenyl-4-(trifluormethyl)-1-(2,4,6-trimethylphenyl)imidazol

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:70276-87-8 SDS

70276-87-8Relevant academic research and scientific papers

Fluorinated heterobutadienes/trimethylphosphine: A reactivity study

Karsch, Hans H.,Leithe, Andreas W.

, p. 1907 - 1911 (2002)

The reactions of fluorinated heterobutadienes F2C=X-C(R)=Y (X = N, CH; Y = O, N-Mes; R = Ph, t-Bu), A-D, with the PMe3 were studied. In any case, a different reaction pathway was observed, depending on the specific nature of A-D. The

Synthesis of Heterocyclic Compounds from 4,4-Bis(trifluoromethyl)-1,3-diazabuta-1,3-dienes, III. Synthesis of Trifluoromethyl Substituted Six Membered Ring Systems by Reaction with Enolethers, Enamines, and Heterocumulenes

Burger, Klaus,Wassmuth, Ulrike,Forster, Barbara,Penninger, Stefan

, p. 1442 - 1452 (2007/10/02)

Regiochemistry and site specifity of cycloaddition reactions of 4,4-bis(trifluoromethyl)-1,3-diazabuta-1,3-dienes with enolethers, enamines and heterocumulenes are described.IR, 1H, 13C, and 19F NMR data of the compounds obtained are discussed. - Key words: Regiochemistry and Site Specifity of Cycloaddition Reactions, Partially Fluorinated Heterocyclic Compounds

Reaction Behaviour of Trifluoromethyl Groups. Synthesis of 1,3-Azoles from Trifluoromethyl-substituted Hetero-1,3-dienes

Burger, Klaus,Ottlinger, Ralph,Goth, Herbert,Firl, Joachim

, p. 2494 - 2507 (2007/10/02)

4,4-Bis(trifluoromethyl)-substituted 1-oxa-3-aza-1,3-butadienes 1, 1-thia-3-aza-1,3-butadienes 2 as well as 1,3-diaza-1,3-butadienes 3 on heating with tin(II) chloride yield 5-fluoro-4-trifluoromethyl-substituted oxazoles 4, thiazoles 5, and imidazoles 6,

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