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3367-02-0

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3367-02-0 Usage

Chemical structure

2-(2-Naphthyl)-1H-benzimidazole is a chemical compound with a benzimidazole core structure substituted with a naphthalene group.

Use as a fluorescent probe

It is used to detect and visualize the presence of metal ions in biological systems.

Potential use in sensing and imaging applications

The compound has been studied for its potential use in sensing and imaging applications, particularly in the field of bioimaging.

Unique structure and properties

Its unique structure and properties make it a promising candidate for the development of new materials and compounds with diverse applications in chemistry and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 3367-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3367-02:
(6*3)+(5*3)+(4*6)+(3*7)+(2*0)+(1*2)=80
80 % 10 = 0
So 3367-02-0 is a valid CAS Registry Number.

3367-02-0SDS

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-naphthalen-2-yl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-naphthalen-2-yl-1H-benzoimidazole

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:3367-02-0 SDS

3367-02-0Relevant articles and documents

Transforming Oxadiazolines through Nitrene Intermediates by Energy Transfer Catalysis: Access to Sulfoximines and Benzimidazoles

Park, Do Dam,Min, Kwan Hong,Kang, Jihee,Hwang, Ho Seong,Soni, Vineet Kumar,Cho, Cheon-Gyu,Cho, Eun Jin

supporting information, p. 1130 - 1134 (2020/02/15)

Subtle differences in reaction conditions facilitated unprecedented photocatalytic reactions of oxadiazolines by energy transfer catalysis. A set of compounds, sulfoximines and benzimidazoles, were ingeniously prepared from oxadiazolines via nitrene intermediates by photocatalytic N-O/C-N bond cleavages. The synthesis of sulfoximines was realized through intermolecular N-S bond formation between nitrene intermediates and sulfoxides, whereas benzimidazoles were obtained via intramolecular aromatic substitution of the nitrene to the tethered aryl substituent.

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