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73673-27-5

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73673-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73673-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73673-27:
(7*7)+(6*3)+(5*6)+(4*7)+(3*3)+(2*2)+(1*7)=145
145 % 10 = 5
So 73673-27-5 is a valid CAS Registry Number.

73673-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diethyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 1H-Imidazole, 4,5-diethyl-

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:73673-27-5 SDS

73673-27-5Downstream Products

73673-27-5Relevant articles and documents

Syntheses of polyalkylated imidazoles

Evjen, Sigvart,Fiksdahl, Anne

supporting information, p. 1392 - 1399 (2017/07/25)

We have developed improved general simple methods for large-scale preparation of polyalkylated imidazoles by improved multicomponent synthesis from commercially available starting materials. A large range of NH- and N-alkyl-polyalkylimidazoles (40 in total, including novel compounds) has been synthesized.

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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