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56653-41-9

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56653-41-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 20 carbon (C) atoms, 17 hydrogen (H) atoms, 3 nitrogen (N) atoms, and 1 oxygen (O) atom.

Explanation

Benzyl derivatives are a group of organic compounds that contain a benzyl group, which is a phenylmethyl group (C6H5-CH2-). This compound belongs to this class due to the presence of a benzyl group in its structure.

Explanation

The compound is a solid at room temperature and has a light yellow color.

Explanation

The molecular weight is the mass of one mole of a substance, calculated by adding the atomic weights of all the atoms in the molecule. In this case, the molecular weight is 315.37 grams per mole.

Explanation

Due to its unique structure and reactivity, 1-(1-Benzyl-1H-benzoimidazol-2-yl)-ethanone is often used as a starting material or intermediate in the synthesis of various pharmaceuticals and other organic compounds.

Explanation

The compound may have potential applications in the field of medicinal chemistry and drug development due to its unique structure and reactivity, which could be exploited to design new drugs or drug candidates.

Explanation

Although the compound has potential applications in various fields, more research and testing are needed to fully understand its properties, reactivity, and potential uses in different applications.

Class

Benzyl derivatives

Structure

Contains a benzimidazole and an ethanone group

Physical State

Light yellow solid

Molecular Weight

315.37 g/mol

Applications

Synthesis of pharmaceuticals and organic compounds

Potential Applications

Medicinal chemistry and drug development

Further Research

Required to fully understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 56653-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,5 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56653-41:
(7*5)+(6*6)+(5*6)+(4*5)+(3*3)+(2*4)+(1*1)=139
139 % 10 = 9
So 56653-41-9 is a valid CAS Registry Number.

56653-41-9SDS

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 1-(1-benzylbenzimidazol-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-phenyl-2-acetylbenzimidazole

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:56653-41-9 SDS

56653-41-9Relevant articles and documents

Carbonylative Acetylation of Heterocycles

Zhang, Youcan,Yin, Zhiping,Wu, Xiao-Feng

, p. 213 - 216 (2020/01/22)

Herein, a new procedure for the carbonylative acetylation of heterocycles has been developed. In this process, organic peroxide acts as the methyl source. Various heterocycles were transformed into the corresponding methyl heterocyclic ketones in moderate to good yields.

A green and simple synthesis of N-alkyl-2-acetylbenzimidazoles

Kumar, P. Kishore,Dubey

experimental part, p. 3249 - 3250 (2012/08/29)

A green and simple synthesis of N-alkyl-2-substituted benzimidazoles has been developed. In this method, 2-acetyl benzimidazole compound (1) was alkylated with reagents such as dimethyl sulfate/diethyl sulfate/benzyl chloride under green conditions i.e., by physical grinding in presence of a mild base like K2CO3 or by using green solvents like PEG-600, ethanol etc. or by using micro-wave irradiation technique to obtain N-alkyl-2-acetylbenzimidazoles compound (2).

Solid phase synthesis of benzimidazole ketones and benzimidazole chalcones under solvent-free conditions

Dubey,Kumar, C. Ravi,Babu, Balaji

, p. 3128 - 3130 (2007/10/03)

Oxidation of 1-alkyl/aralkyl-2-(α-hydroxyalkyl/aryl)benzimidazoles 1 with KMnO4 on neutral alumina under solid phase conditions gives the corresponding ketones, 1-alkyl/aralkyl-2-acyl-benzimidazoles 2. Compound 2a (R2 = CH3) on condensation with aromatic aldehydes in the presence of solid NaOH under solvent-free conditions, yields the corresponding chalcones, 1-alkyl/aralkyl-2-benzimidazole aryl vinyl ketone 3.

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