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161095-84-7

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161095-84-7 Usage

Structure

A derivative of imidazole with a substituted methyl group and a propenyl group attached to the carbon atoms

Classification

Imidazole compound

Physical state

Colorless liquid at room temperature

Usage

Commonly used in organic synthesis and pharmaceutical research

Purpose

Suitable for use as a reagent in various chemical reactions and has potential applications in the development of pharmaceutical drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 161095-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,0,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161095-84:
(8*1)+(7*6)+(6*1)+(5*0)+(4*9)+(3*5)+(2*8)+(1*4)=127
127 % 10 = 7
So 161095-84-7 is a valid CAS Registry Number.

161095-84-7SDS

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 1H-Imidazole,1-methyl-4-(1-methyl-1-propenyl)-,(E)-(9CI)

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:161095-84-7 SDS

161095-84-7Upstream product

161095-84-7Downstream Products

161095-84-7Relevant articles and documents

A Two-Step Synthesis of Imidazoles from Aldehydes via 4-Tosyloxazolines

Horne, David A.,Yakushijin, Kenichi,Buechi, George

, p. 139 - 154 (2007/10/02)

Imidazoles with substituents in the 4- and 4,5-positions were prepared by heating 4-tosyloxazolines in saturated methanolic ammonia.Similar treatment of these oxazolines with monoalkylamines regioselectively affords 1,4-disubstituted imidazoles.When oxazolines bearing an ethyl group at the 4-position were heated with alkylamines, however, a regioisomeric mixture of di- or trisubstituted imidazoles was produced.These reactions proceed via an intermolecular condensation of α-amino ketones and amidines or intramolecular cyclization of α-amidino ketone intermediates, respectively.

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