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2-(4-FLUORO-PHENYL)-1-METHYL-1H-IMIDAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

385442-12-6

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385442-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 385442-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,5,4,4 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 385442-12:
(8*3)+(7*8)+(6*5)+(5*4)+(4*4)+(3*2)+(2*1)+(1*2)=156
156 % 10 = 6
So 385442-12-6 is a valid CAS Registry Number.

385442-12-6SDS

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-(4-fluorophenyl)-1-methyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-(4-fluorophenyl)-1-methylimidazole

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:385442-12-6 SDS

385442-12-6Relevant academic research and scientific papers

Iron catalyzed oxidative assembly of N-heteroaryl and aryl metal reagents using oxygen as an oxidant

Liu, Kun Ming,Liao, Lian Yan,Duan, Xin Fang

supporting information, p. 1124 - 1127 (2015/01/09)

An equivalent amount of N-heteroaryl and aryl Grignard or lithium reagents, after mediation by an equivalent of titanate, was facilely coupled to furnish N-heteroaryl-aryl compounds under the catalysis of FeCl3/TMEDA at ambient temperature using oxygen as an oxidant. Most of the common N-heteroaryls were all good candidates, and thus provided a general, green and pratical protocol for the flexible construction of various N-heteroaryl-aryl structures. This journal is

N -heterocyclic carbene-palladium(II)-1-methylimidazole complex-catalyzed direct C-H bond arylation of (Benz)imidazoles with aryl chlorides

Gu, Zheng-Song,Chen, Wen-Xin,Shao, Li-Xiong

, p. 5806 - 5811 (2014/07/08)

(Benz)imidazoles can be efficiently functionalized by (hetero)aryl chlorides via direct C-H bond arylation in the presence of a well-defined NHC-Pd(II)-Im complex. Under the optimal conditions, various activated, unactivated, and deactivated (hetero)aryl chlorides were successfully applied as the arylating reagents to achieve the 2-(hetero)aryl (benz)imidazoles in acceptable to high yields, giving a facile and alternative methodology for the direct C-H bond arylation of (benz)imidazoles.

Phosphines with 2-imidazolium and para-phenyl-2-imidazolium moieties - Synthesis and application in two-phase catalysis

Brauer, David J.,Kottsieper, Konstantin W.,Liek, Christian,Stelzer, Othmar,Waffenschmidt, Horst,Wasserscheid, Peter

, p. 177 - 184 (2007/10/03)

Deprotonation of 1-n-butyl-3-methyl-imidazolium chloride or hexafluorophosphate with n-butyl lithium and subsequent reaction of the intermediate 2,3-dihydro-imidazol-2-ylidene with diphenylchlorophosphine affords the 2-imidazolium phosphines 3a or 3b. The

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