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56048-67-0 Usage

Molecular Structure

2-(naphthalen-1-yl)-2,3-dihydro-1,3-benzothiazole has a complex molecular structure that includes a naphthalene ring and a benzothiazole group.


It is a heterocyclic compound, which means it contains at least one ring with one or more non-carbon atoms.

Potential Applications

It has potential pharmaceutical applications and has been studied for its potential use in the development of drugs for various medical conditions, including neurological disorders and cancer.

Medicinal Chemistry

Its unique structure and potential biological activities make it an interesting target for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 56048-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,4 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56048-67:
130 % 10 = 0
So 56048-67-0 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 2-naphthalen-1-yl-2,3-dihydro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-naphthalen-1-yl-2,3-dihydro-benzothiazole

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:56048-67-0 SDS

56048-67-0Relevant articles and documents

Enantioselective organocatalytic transfer hydrogenation of α-imino esters by utilization of benzothiazoline as highly efficient reducing agent

Zhu, Chen,Akiyama, Takahiko

supporting information; experimental part, p. 1846 - 1850 (2010/11/03)

Benzothiazoline was employed as an efficient and versatile reducing agent for the chiral phosphoric acid-catalyzed transfer hydrogenation of α-imino esters. The corresponding α-amino esters were furnished with excellent enantioselectivities. Novel and rea

Control of acarids using certain benzothiazoles or benzothiazolines


, (2008/06/13)

Compounds having either of the structures SPC1 Have strong acaricidal activity, in which R is a phenyl or naphthyl group, or phenyl with certain designated substitution. Thus, mites may be controlled on such crops as cotton by applying such compounds as 2-(1-naphthyl)benzothiazoline or 2-(5-t-butyl-2-hydroxyphenyl)benzothiazole.

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