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Benzenamine, 4-(2-phenyl-1H-imidazol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

850338-87-3

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850338-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 850338-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,3,3 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 850338-87:
(8*8)+(7*5)+(6*0)+(5*3)+(4*3)+(3*8)+(2*8)+(1*7)=173
173 % 10 = 3
So 850338-87-3 is a valid CAS Registry Number.

850338-87-3SDS

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 4-(2-phenyl-1H-1-imidazolyl)aniline

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:850338-87-3 SDS

850338-87-3Downstream Products

850338-87-3Relevant academic research and scientific papers

Design, synthesis, and gas permeation properties of polyimides containing pendent imidazolium groups

Shrimant, Bharat,Kharul, Ulhas K.,Wadgaonkar, Prakash P.

, p. 1721 - 1729 (2018/07/03)

Film-forming polymers containing ionic groups have attracted considerable attention as emerging materials for gas separation applications. The aim of this article was to synthesize new film-forming polyimides containing imidazolium groups (PI-IMs) and est

P2X4 RECEPTOR ANTAGONIST

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Paragraph 0087, (2016/08/17)

The present invention relates to a compound represented by the following general formula (II), wherein, in the formula, R1a to R6a represent hydrogen atom, an alkyl group having 1 to 8 carbon atoms, and the like, Xa repres

Synthesis, structure-activity relationships at the GABAA receptor in rat brain, and differential electrophysiological profile at the recombinant human GABAA receptor of a series of substituted 1,2-diphenylimidazoles

Asproni, Battistina,Talani, Giuseppe,Busonero, Fabio,Pau, Amedeo,Sanna, Sebastiano,Cerri, Riccardo,Mascia, Maria Paola,Sanna, Enrico,Biggio, Giovanni

, p. 2638 - 2645 (2007/10/03)

A series of new 1,2-diphenylimidazole derivatives (1a-x) were synthesized and evaluated for their ability to potentiate γ-aminobutyric acid (GABA)-evoked currents in Xenopus laevis oocytes expressing recombinant human GABAA receptors. Many of t

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