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5-[3-(octylsulfanyl)propyl]-1,3-benzodioxole is a complex organic chemical compound characterized by a benzodioxole ring, which is a benzene ring with two oxygen atoms forming a dioxole structure. The compound features an octylsulfanyl (octylthio) group attached to a propyl chain, which is further connected to the benzodioxole ring. This structure contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's specific arrangement of atoms and functional groups may influence its reactivity, solubility, and interaction with other molecules, making it a subject of interest for chemical research and development.

5570-95-6

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5570-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5570-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5570-95:
(6*5)+(5*5)+(4*7)+(3*0)+(2*9)+(1*5)=106
106 % 10 = 6
So 5570-95-6 is a valid CAS Registry Number.

5570-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[3-(octylsulfanyl)propyl]-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 5-(3-octylmercapto-propyl)-benzo[1,3]dioxole

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:5570-95-6 SDS

5570-95-6Downstream Products

5570-95-6Relevant academic research and scientific papers

Ex Situ Formation of Methanethiol: Application in the Gold(I)-Promoted Anti-Markovnikov Hydrothiolation of Olefins

Kristensen, Steffan K.,Laursen, Simon L. R.,Taarning, Esben,Skrydstrup, Troels

supporting information, p. 13887 - 13891 (2018/10/02)

A protocol for the Au-promoted anti-Markovnikov hydrothiolation of olefins using ex situ generated methanethiol is reported. The use of S-methylisothiourea hemisulfate salt as a solid precursor for methanethiol generation ensures a safe and reliable deliverance of a stoichiometric amount of this thiol. The procedure was shown to work for a broad range of olefins providing the corresponding hydrothiolated adduct in good to excellent yields. Mechanistic evaluations suggest that thiyl radicals are generated and that gold acts as an efficient but stable radical initiator.

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