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2-phenyl-2-propyl-1,3-dithiolane is an organic compound characterized by a unique structure that includes a 1,3-dithiolane ring, which is a five-membered ring containing two sulfur atoms. The molecule features a phenyl group (a benzene ring) and a propyl chain attached to the same carbon atom of the dithiolane ring. This specific arrangement endows the compound with distinct chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. The compound's molecular formula is C11H14S2, reflecting its composition of carbon, hydrogen, and sulfur atoms.

5769-03-9

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5769-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5769-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5769-03:
(6*5)+(5*7)+(4*6)+(3*9)+(2*0)+(1*3)=119
119 % 10 = 9
So 5769-03-9 is a valid CAS Registry Number.

5769-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-2-propyl-1,3-dithiolane

1.2 Other means of identification

Product number -
Other names 1,3-DITHIOLANE,2-PHENYL-2-PROPYL

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:5769-03-9 SDS

5769-03-9Relevant academic research and scientific papers

An efficient, continuous flow technique for the chemoselective synthesis of thioacetals

Wiles, Charlotte,Watts, Paul,Haswell, Stephen J.

, p. 7362 - 7365 (2008/03/13)

By optimizing a reagent's residence time within a packed-bed reactor, it is possible to overcome selectivity issues frequently encountered in stirred reaction vessels. This important feature is demonstrated for the chemoselective protection of 4-acetylben

Silica gel-supported polyphosphoric acid (PPA/SiO2) as an efficient and reusable catalyst for conversion of carbonyl compounds into oxathioacetals and dithioacetals

Aoyama, Tadashi,Takido, Toshio,Kodomari, Mitsuo

, p. 2307 - 2310 (2007/10/03)

A simple and efficient method for the conversion of carbonyl compounds to oxathioacetals and dithioacetals by using polyphosphoric acid supported on silica gel (PPA/SiO2) as an acid catalyst have been developed. PPA/SiO2 is easily re

Chemoselective Protection of Carbonyl Compounds as Dithioacetals Using Silica Gel Supported Aluminium Chloride

Tamami,Borujeny, K. Parvanak

, p. 4253 - 4258 (2007/10/03)

Silica gel supported aluminium chloride is shown to be a mild chemoselective catalyst for dithioacetalization of carbonyl compounds.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Robbe,Fernandez,Dubief,et al.

, p. 235 - 243 (2007/10/02)

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.

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