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42032-30-4

42032-30-4

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42032-30-4 Usage

General Description

1-Decyl-2-methylimidazole is an 1-alkyl-2-methylimidazole. It participates in the extraction process of Cu(II) complexes.

Check Digit Verification of cas no

The CAS Registry Mumber 42032-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42032-30:
(7*4)+(6*2)+(5*0)+(4*3)+(3*2)+(2*3)+(1*0)=64
64 % 10 = 4
So 42032-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H26N2/c1-3-4-5-6-7-8-9-10-12-16-13-11-15-14(16)2/h11,13H,3-10,12H2,1-2H3

42032-30-4 Well-known Company Product Price

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  • Aldrich

  • (433799)  1-Decyl-2-methylimidazole  97%

  • 42032-30-4

  • 433799-25ML

  • 1,371.24CNY

  • Detail

42032-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-DECYL-2-METHYLIMIDAZOLE

1.2 Other means of identification

Product number -
Other names 1-Decyl-2-methyl-1H-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:42032-30-4 SDS

42032-30-4Relevant articles and documents

Synthesis of N-alkylated derivatives of imidazole as antibacterial agents

Khabnadideh,Rezaei,Khalafi-Nezhad,Bahrinajafi,Mohamadi,Farrokhroz

, p. 2863 - 2865 (2007/10/03)

N-Alkylation of imidazole, 2-methylimidazole and 2-methyl-4-nitroimidazole have been carried out to achieve effective antibacterial agents. The products were then investigated for antibacterial activity against Escherichia coil, Staphylococcus aureus and Pseudomonas aeruginosa. Antibacterial effects of 1-alkylimidazole derivatives increase as the number of carbons in alkyl chain increases up to nine carbons. Also substitution of 2-methyl and 2-methyl-4-nitro groups on imidazole ring increases the antibacterial activity.

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