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2,4,6-tris(4-methoxyphenyl)-1,3,5-trithiane is a complex organic compound characterized by its unique structure, which consists of a central trithiane core (a sulfur-containing ring system) with three 4-methoxyphenyl groups attached to each of the sulfur atoms. 2,4,6-tris(4-methoxyphenyl)-1,3,5-trithiane is known for its potential applications in various fields, such as materials science and pharmaceuticals, due to its interesting electronic and steric properties. The presence of the methoxy groups on the phenyl rings can influence the compound's solubility and reactivity, making it a subject of interest for chemists studying the effects of functional group substitution on molecular behavior.

5692-49-9

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5692-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5692-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5692-49:
(6*5)+(5*6)+(4*9)+(3*2)+(2*4)+(1*9)=119
119 % 10 = 9
So 5692-49-9 is a valid CAS Registry Number.

5692-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(4-methoxyphenyl)-1,3,5-trithiane

1.2 Other means of identification

Product number -
Other names Trithioanisaldehyde

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:5692-49-9 SDS

5692-49-9Relevant academic research and scientific papers

A new convenient procedure for the thionation of carbonyl compounds utilizing tetrachlorosilane-sodium sulfide

Salama, Tarek A.,El-Ahl, Abdel-Aziz S.,Elmorsy, Saad S.,Khalil, Abdel-Galil M.,Ismail, Mohamed A.

experimental part, p. 5933 - 5936 (2010/01/11)

A combination of tetrachlorosilane (TCS) and sodium sulfide in acetonitrile is found to be an efficient thionating reagent for aromatic aldehydes in the absence of catalysis to give the corresponding thioaldehydes as trimers in good yields. Under cobalt(I

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