89738-83-0

Basic information

• Product Name: 1,2-Ethanedithiol, 1,2-bis[2,4,6-tris(1,1-dimethylethyl)phenyl]-
• CAS NO: 89738-83-0
• Molecular Formula: C38H62S2
• Molecular Weight: 583.042
• Mol File: 89738-83-0.mol

Chemical Properties

• CAS DataBase Reference: 1,2-Ethanedithiol, 1,2-bis[2,4,6-tris(1,1-dimethylethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Ethanedithiol, 1,2-bis[2,4,6-tris(1,1-dimethylethyl)phenyl]-(89738-83-0)
• EPA Substance Registry System: 1,2-Ethanedithiol, 1,2-bis[2,4,6-tris(1,1-dimethylethyl)phenyl]-(89738-83-0)

Safety Data

• Hazardous Substances Data: 89738-83-0(Hazardous Substances Data)

Upstream product

• 3975-77-7 1-bromo-2,4,6-tri-tert-butylbenzene 
• 84543-57-7 2,4,6-tri-(tert-butyl)thiobenzaldehyde 
• 594-19-4 tert.-butyl lithium 
• 677-22-5 tert-butylmagnesium chloride 
• 917-64-6 methyl magnesium iodide 
• 917-54-4 methyllithium 

Relevant articles and documents

Synthesis, Structure, and Some Reactions of (2,4,6-Tri-t-butyl)thiobenzaldehyde, the First Stable Aromatic Thioaldehyde

The title compound 1 was synthesized by the reaction of 2,4,6-tri-t-butylphenyllithium with O-ethyl thioformate or that of 2,4,6-tri-t-butylbenzaldehyde hydrazone with disulfur dichloride in the presence of triethylamine. The thioaldehyde 1 is a purple cr

NEW ASPECTS OF ORGANOSELENIUM COMPOUNDS CONTAINING GROUP 14 ELEMENTS

The synthesis and reactivities of double bond compounds between Group 14 and Group 16 elements have been reported.Specifically the chemistry of M=X type compounds (C=Se, Ge=S, Sn=S, Sn=Se) are described.

REACTIONS OF A STABLE THIOBENZALDEHYDE WITH ORGANOMETALLICS

Rections of 2,4,6-tri-t-butylthiobenzaldehyde with Grignard and organolithium reagents gave products via the anion radical of the thioaldehyde.The first example of dimerization of thioketyl radicals was also presented.