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5060-70-8

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5060-70-8 Usage

Chemical composition

Composed of a naphthalene core with an octadecylsulfanyl chain.

Usage

Commonly used in the production of lubricants, surfactants, and other industrial applications.

Property 1

Alkylthio-substituted aromatic compound.

Property 2

Exhibits excellent hydrophobic and lipophilic properties.

Benefit

Useful in formulations requiring water repellency, such as manufacturing waterproof coatings or creating stable emulsions.

Aromatic nature

May make it suitable for use as a fragrance ingredient or in chemical synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5060-70-8 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, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5060-70:
(6*5)+(5*0)+(4*6)+(3*0)+(2*7)+(1*0)=68
68 % 10 = 8
So 5060-70-8 is a valid CAS Registry Number.

5060-70-8SDS

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-octadecylsulfanylnaphthalene

1.2 Other means of identification

Product number -
Other names 2-(octadecylsulfanyl)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:5060-70-8 SDS

5060-70-8Downstream Products

5060-70-8Relevant articles and documents

Nickel-Catalyzed C?S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters

Lee, Shao-Chi,Liao, Hsuan-Hung,Chatupheeraphat, Adisak,Rueping, Magnus

supporting information, p. 3608 - 3612 (2018/03/13)

A nickel catalyzed cross-coupling protocol for the straightforward C?S bond formation has been developed. Various mercaptans and a wide range of ester and amide substrates bearing various substituents were tolerated in this process which afforded products in good to excellent yields. Furthermore, an intramolecular protocol for the synthesis of thioethers starting from thioesters has been developed. The utility of this protocol has been demonstrated in a new synthetic protocol of benzothiophene.

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