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1H-Benzimidazole, 2-(3-butenyl)-(9CI) is an organic compound with the chemical formula C9H10N2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The 2-(3-butenyl) substitution refers to the presence of a 3-butenyl group attached to the 2-position of the benzimidazole core. 1H-Benzimidazole,2-(3-butenyl)-(9CI) is characterized by its unique chemical structure, which contributes to its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its specific functional groups and molecular arrangement, 1H-Benzimidazole, 2-(3-butenyl)-(9CI) may exhibit distinct chemical properties and reactivity compared to other benzimidazole derivatives.

5838-57-3

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5838-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5838-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5838-57:
(6*5)+(5*8)+(4*3)+(3*8)+(2*5)+(1*7)=123
123 % 10 = 3
So 5838-57-3 is a valid CAS Registry Number.

5838-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(but-3-en-1-yl)-1H-benzo[d]imidazole

1.2 Other means of identification

Product number -
Other names 4-(2-Benzimidazolyl)-1-buten

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:5838-57-3 SDS

5838-57-3Relevant academic research and scientific papers

Additive-free pd-catalyzed α-allylation of imine-containing heterocycles

Kljajic, Marko,Puschnig, Johannes G.,Weber, Hansj?rg,Breinbauer, Rolf

supporting information, p. 126 - 129 (2017/11/27)

An additive-free Pd-catalyzed α-allylation of different imino-group-ontaining heterocycles is reported. The activation of α-CH pronucleophiles (pKa (DMSO) > 25) occurs without the addition of strong bases or Lewis acids using only the Pd/Xantphos catalyst system. The reaction scope has been studied for various 5- and 6-membered nitrogen-containing heterocycles (yields up to 96%). Mechanistic investigations suggest an initial allylation of the imine-N followed by a Pd-catalyzed formal aza-Claisen rearrangement.

Functionalized orthoesters as powerful building blocks for the efficient preparation of heteroaromatic bicycles

Bastug, Gulluzar,Eviolitte, Christophe,Markó, István E.

supporting information; experimental part, p. 3502 - 3505 (2012/08/08)

By combining substituted anilines with functionalized orthoesters, an efficient and connective methodology for the preparation of benzoxazole, benzothiazole, and benzimidazole derivatives has been established. The versatility of this approach enables the development of new libraries of heterocycles containing multifunctional sites.

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