63877-57-6

Basic information

• Product Name: Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-
• CAS NO: 63877-57-6
• Molecular Formula: C15H24O3S
• Molecular Weight: 284.42
• Mol File: 63877-57-6.mol
• Article Data: 8

Chemical Properties

• Density: 1.083±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-(63877-57-6)
• EPA Substance Registry System: Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-(63877-57-6)

Safety Data

• Hazardous Substances Data: 63877-57-6(Hazardous Substances Data)

Upstream product

• 6553-96-4 2,4,6-triisopropylphenylsulfonyl chloride 
• 82965-03-5 2,4,6-triisopropyl-benzenesulfonic acid n-hexylester 
• 717-74-8 1,3,5-triisopropyl benzene 

Downstream Products

• 80524-41-0 2,4,6-Triisopropyl-benzenesulfonic acid 2-oxo-pentyl ester 
• 143585-49-3 (1R,2R)-N,N'-bis(2,4,6-triisopropylbenzenesulfonyl)-cyclohexane-1,2-diamine 
• 1107634-93-4 silver(I) 2,4,6-tri(iso-propyl)benzenesulfonate 

Relevant articles and documents

Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates

Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds.

A [4+4] annulation strategy for the synthesis of eight-membered carbocycles based on intramolecular cycloadditions of conjugated enynes

A [4+4] annulation strategy for the synthesis of eight-membered carbocycles is reported that proceeds via a cascade involving two pericyclic processes. In the first step, the [4+2] cycloaddition of a conjugated enyne with an electron-deficient cyclobutene

Reactivity of sterically hindered aromatic sulfonic acid derivatives: VII.* hydrolysis of arenesulfonyl chlorides in aqueous acetonitrile

Hydrolysis of sterically hindered arenesulfonyl chlorides in aqueous acetonitrile is accelerated by both electron-acceptor and some electron-donor substituents in the benzene ring. A multifactor kinetic model of the process is proposed. 1998 MAHK Hayka/Interperiodica Publishing.