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2-tridecyl-1H-benzimidazole is a chemical compound with the molecular formula C20H27N2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The "2-tridecyl" part of the name indicates that there is a 13-carbon alkyl chain (tridecyl) attached to the 2-position of the benzimidazole ring. 2-tridecyl-1H-benzimidazole is known for its antimicrobial properties and is commonly used as a preservative in various products, including cosmetics and personal care items, to prevent the growth of bacteria, yeasts, and molds. Its effectiveness as a biocide is attributed to its ability to disrupt cell membrane integrity and interfere with essential enzymatic processes in microorganisms.

5805-25-4

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5805-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5805-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5805-25:
(6*5)+(5*8)+(4*0)+(3*5)+(2*2)+(1*5)=94
94 % 10 = 4
So 5805-25-4 is a valid CAS Registry Number.

5805-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tricyanovinylpyrrole

1.2 Other means of identification

Product number -
Other names 2-(Tricyanovinyl)-pyrrol

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:5805-25-4 SDS

5805-25-4Downstream Products

5805-25-4Relevant academic research and scientific papers

Enzyme-mediated domino synthesis of 2-alkylbenzimidazoles in solvent-free system: A green route to heterocyclic compound

Wang, Li,Li, Chao,Wang, Na,Li, Kun,Chen, Xi,Yu, Xiao-Qi

body text, p. 16 - 20 (2010/12/19)

Solvent-free domino acylation/cyclization reactions between fatty acid esters and o-phenylenediamine mediated by immobilized lipase from Mucor miehei (MML) were found to be an efficient way in the synthesis of 2- alkylbenzimidazole. Compared with other substrates, methyl fatty acid esters with moderated chain length exhibited best activity with yield up to 95%. The mechanism of the domino process was clarified deeply through some detail experiments, including separation of intermediates. This efficient enzymatic domino process provides an attractive procedure for heterocyclic compound synthesis and could be regarded as a potential synthetic method in modern organic chemistry.

Synthesis and insecticidal activity of some benzimidazolic and benzothiazolic derivatives

Lahlou, M.,Weliou, M.,Salem, M.,Hajji, M. S.

, p. 57 - 61 (2007/10/03)

The benzimidazolic and benzothiazolic derivatives with a (CH2)n radical in 2 position of the heterocycle had been synthesized and then tested for their insecticidal activity on Culex pipiens larvae. The benzothiazolic derivatives were found to be the most active. The study has also showed that this activity was related to the nature of the substitute in 2 position of the heterocycle. This activity increased when (CH2)n chain increased until n = 6; above this value, the activity decreased.

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