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56048-50-1

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56048-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56048-50-1 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56048-50:
(7*5)+(6*6)+(5*0)+(4*4)+(3*8)+(2*5)+(1*0)=121
121 % 10 = 1
So 56048-50-1 is a valid CAS Registry Number.

56048-50-1SDS

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-1-yl-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-(1-naphthyl)-1,3-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:56048-50-1 SDS

56048-50-1Relevant articles and documents

Synthesis, photo- and electro-luminescence of red-emitting Ir(III) complexes with 2-(1-naphthyl)benzothiazole and carrier transporting group-functionalized picolinate ligands

Yu, Tianzhi,Bao, Yanjun,Zhao, Yuling,Zhang, Hui,Xu, Zixuan,Wu, Xiaomeng

, p. 33 - 40 (2016)

Two new red-emitting Ir(III) complexes containing 2-(1-naphthyl)benzothiazole as cyclometalated ligands and the carrier transporting group-functionalized picolinate as ancillary ligands have been successfully synthesized and characterized. The Ir(III) complexes have good thermal stability with less than 2% weight-reduction occurring at 285 °C, and exhibit strong red emissions. The doped light-emitting devices using the Ir(III) complexes as dopants were fabricated. The result indicated that the light-emitting devices fabricated by the carbazole-functionalized complex and the diaryl-1,3,4-oxadiazole-functionalized complex exhibited red emissions with a maximum brightness of 3074 and 2520 cd/m2at 10.7 V and a maximum current efficiency of 4.84 and 5.18 cd/A, respectively.

Room temperature HFIP/Ag-promoted palladium-catalyzed C–H functionalization of benzothiazole with iodoarenes

Bhujbal, Yuvraj,Gharpure, Santosh J.,Kapdi, Anant R.,Kommyreddy, Saidurga Prasad,Kori, Santosh,Vadagaonkar, Kamlesh

supporting information, p. 847 - 850 (2022/02/01)

A versatile synthetic protocol involving the room temperature direct arylation of benzothiazole with a wide variety of iodoarenes under Ag-promoted Pd-catalyzed conditions in HFIP as the reaction solvent has been presented. A sequential HFIP-promoted sele

Ultrasound-assisted efficient and green synthesis of 2-substituted benzothiazoles under solvent-free condition using recyclable sulfated tungstate

Pise, Ashok S.,Ingale, Ajit P.,Dalvi, Navnath R.

supporting information, p. 3629 - 3641 (2021/10/12)

Sulfated tungstate catalyzed an efficient and ecofriendly protocol has been described for the synthesis of 2-substituted benzothiazoles. The corresponding benzothiazoles were obtained using a condensation reaction of 2-aminothiophenol with various aldehydes under ultrasound irradiation at room temperature. Various functional groups on the 2-aminothiophenol as well as on the aldehydes were tolerated to provide 2-substituted benzothiazoles derivatives in excellent yields. The faster reaction rate, solvent-free or mild reaction conditions, wide functional group compatibility, excellent yields, easy work-up procedure, and excellent catalyst recyclability are the advantages of this protocol. These advantages make this process more practicable, cost-effective, and environmentally benign.

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