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2-(decylsulfanyl)naphthalene, also known as 2-naphthalenethiol or 2-benzothiophene, is a chemical compound belonging to the naphthalene family, characterized by a sulfur atom attached to a decyl group. With a molecular formula of C16H18S, it is a yellowish solid that emits a strong, unpleasant odor. Due to its hazardous nature and potential irritancy to the skin, eyes, and respiratory system, it requires careful handling and storage.

5060-68-4

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5060-68-4 Usage

Uses

Used in Organic Synthesis:
2-(decylsulfanyl)naphthalene is utilized as a starting material in the synthesis of various organic compounds and polymers, contributing to the development of a wide range of chemical products.
Used in Dye Production:
In the dye industry, 2-(decylsulfanyl)naphthalene is employed as a key component in the production of dyes, owing to its chemical properties that facilitate the creation of diverse colorants.
Used in Pharmaceutical Industry:
2-(decylsulfanyl)naphthalene is used as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medicinal compounds.
Used in Pesticide Production:
In agriculture, 2-(decylsulfanyl)naphthalene is applied in the manufacturing process of pesticides, serving as a vital precursor for the creation of effective crop protection agents.

Check Digit Verification of cas no

The CAS Registry Mumber 5060-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5060-68:
(6*5)+(5*0)+(4*6)+(3*0)+(2*6)+(1*8)=74
74 % 10 = 4
So 5060-68-4 is a valid CAS Registry Number.

5060-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-decylsulfanylnaphthalene

1.2 Other means of identification

Product number -
Other names 2-(decylsulfanyl)naphthalene

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:5060-68-4 SDS

5060-68-4Downstream Products

5060-68-4Relevant academic research and scientific papers

Mono- And Dinuclear α-Diimine Nickel(II) and Palladium(II) Complexes in C-S Cross-Coupling

Talukder, Md Muktadir,Miller, Justin T.,Cue, John Michael O.,Udamulle, Chinthaka M.,Bhadran, Abhi,Biewer, Michael C.,Stefan, Mihaela C.

, p. 83 - 94 (2021/01/14)

The usefulness of transition metal catalytic systems in C-S cross-coupling reactions is significantly reduced by air and moisture sensitivity, as well as harsh reaction conditions. Herein, we report four highly air- and moisture-stable well-defined mononuclear and bridged dinuclear α-diimine Ni(II) and Pd(II) complexes for C-S cross-coupling. Various ligand frameworks, including acenaphthene- and iminopyridine-based ligands, were employed, and the resulting steric properties of the catalysts were evaluated and correlated with reaction outcomes. Under aerobic conditions and low temperatures, both Ni and Pd systems exhibited broader substrate scope and functional group tolerance than previously reported catalysts. Over 40 compounds were synthesized from thiols containing alkyl, benzyl, and heteroaryl groups. Also, pharmaceutically active heteroaryl moieties are incorporated from thiol and halide sources. Notably, the bridged dinuclear five-coordinate Ni complex has outperformed the remaining three mono four- or six-coordinate complexes by giving almost quantitative yields across a broad substrate scope.

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