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7570-97-0

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7570-97-0 Usage

General Description

2-(benzylsulfanyl)naphthalene is a chemical compound that belongs to the class of organic compounds known as aromatic thiophenes. It is a sulfur-containing heterocyclic compound with a naphthalene core, and is commonly used as a precursor in the synthesis of various organic compounds and pharmaceuticals. The benzylsulfanyl group attached to the naphthalene ring confers unique chemical and pharmacological properties to the compound, making it valuable for medicinal and industrial applications. However, it is important to handle this chemical with care due to its potential hazards and toxic properties. Overall, 2-(benzylsulfanyl)naphthalene is a versatile compound with a range of potential uses in the fields of chemistry, medicine, and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 7570-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7570-97:
(6*7)+(5*5)+(4*7)+(3*0)+(2*9)+(1*7)=120
120 % 10 = 0
So 7570-97-0 is a valid CAS Registry Number.

7570-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylsulfanylnaphthalene

1.2 Other means of identification

Product number -
Other names benzyl 2-naphthyl sulfide

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:7570-97-0 SDS

7570-97-0Relevant articles and documents

Synthesis of benzyl thioether derivatives via N-heterocyclic carbene palladium(II)-catalyzed cross coupling of benzylammonium salts with thiophenols

Wang, Tao,Guo, Jiarui,Xu, Yongli,Wang, Xiaobo,Wang, Yan,Feng, Dandan,Liu, Lantao

, (2021/12/01)

A new route to benzyl thioether derivatives has been developed via the N-heterocyclic carbene palladium(II)-catalyzed cross coupling of benzylammonium salts with thiophenols. Under the optimal conditions, different benzylammonium salts could be well toler

Transition-Metal-Free and Base-Promoted Carbon-Heteroatom Bond Formation via C-N Cleavage of Benzyl Ammonium Salts

Liu, Long,Tang, Yuanyuan,Wang, Kunyu,Huang, Tianzeng,Chen, Tieqiao

, p. 4159 - 4170 (2021/03/09)

A facile and general method for constructing carbon-heteroatom (C-P, C-O, C-S, and C-N) bonds via C-N cleavage of benzyl ammonium salts under transition-metal-free conditions was reported. The combination of t-BuOK and 18-crown-6 enabled a wide range of substituted benzyl ammonium salts to couple readily with different kinds of heteroatom nucleophiles, i.e. hydrogen phosphoryl compounds, alcohols, thiols, and amines. Good functional group tolerance was demonstrated. The scale-up reaction and one-pot synthesis were also successfully performed.

Synthesis and characterization of Pd(II) complexes bearing NS, CS, SNS and SCS ligands. Evaluation of their microwave assisted catalytic activity in C–C coupling reactions

Aguilar-Castillo, Bethsy A.,Gabriel Flores-Rojas, G.,González-Sebastián, Lucero,Hernández-Ortega, Simón,Morales-Morales, David,Reyes-Martínez, Reyna

, (2020/05/29)

A series of coordination (Pd-NS, Pd-SNS, Pd-SNS-O) and organometallic (Pd-C and Pd-SCS) Pd(II) complexes supported by bidentate and tridentate ligands featuring sulphur moieties have been prepared. All ligands and their palladium complexes were fully char

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