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N-methyl-2-(1-adamantyl)imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77139-82-3

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77139-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77139-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77139-82:
(7*7)+(6*7)+(5*1)+(4*3)+(3*9)+(2*8)+(1*2)=153
153 % 10 = 3
So 77139-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2/c1-16-3-2-15-13(16)14-7-10-4-11(8-14)6-12(5-10)9-14/h2-3,10-12H,4-9H2,1H3

77139-82-3SDS

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 2-(1-adamantyl)-1-methylimidazole

1.2 Other means of identification

Product number -
Other names Imidazole,2-(1-adamantyl)-1-methyl

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:77139-82-3 SDS

77139-82-3Downstream Products

77139-82-3Relevant academic research and scientific papers

Adamantane derivatives of biological interest. Synthesis and antiviral activity of 2-(1-adamantyl)imidazole derivatives

Pellicciari,Fioretti,Cogolli,Tiecco

, p. 2103 - 2105 (2007/10/02)

The methods of synthesis and antiviral evaluation of 2-(1-adamantyl)imidazole (2a), N-methyl-2-(1-adamantyl)imidazole (2b) and 2-(1-adamantyl)benzimidazole (3a) are reported. These compounds are prepared by the selective homolytic substitution reaction by the adamantyl radical (Ad.) on the C-2 carbon atom of the heterocycles. Ad. radicals were generated by oxidative decarboxylation of 1-adamantyl carboxylic acid. Antiviral activities of compounds 2a, 2b and 3a were tested in chick embryos against A-2 Victoria virus. Compounds 2a and 2b showed significant antiviral activity, whereas compound 3a was found inactive.

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