93088-62-1

Basic information

• Product Name: 2,3-dimethylbutyl 4-methylbenzenesulfonate
• CAS NO: 93088-62-1
• Molecular Weight: 256.366
• Mol File: 93088-62-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3-dimethylbutyl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethylbutyl 4-methylbenzenesulfonate(93088-62-1)
• EPA Substance Registry System: 2,3-dimethylbutyl 4-methylbenzenesulfonate(93088-62-1)

Safety Data

• Hazardous Substances Data: 93088-62-1(Hazardous Substances Data)

Upstream product

• 563-78-0 2,3-Dimethyl-1-butene 
• 108-64-5 Ethyl isovalerate 
• 54004-42-1 2,3-dimethyl-butanoic acid, ethyl ester 
• 14287-61-7 2,3-dimethylbutyric acid 
• 503-74-2 3-methylbutyric acid 
• 19550-30-2 2,3-dimethylbutanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 58447-69-1 2-methyl-2-isopropyl malonic acid diethyl ester 
• 51760-90-8 2,3-dimethylbutyryl chloride 

Downstream Products

• 91638-67-4 (2,3-dimethylbutyl)(phenyl)sulfane 
• 68702-73-8 rac-(2,3-Dimethylbutyl)triphenylphosphonium iodide 
• 134553-24-5 C₃₈H₅₆O₆S 
• 134511-53-8 2,3-dimethylbutyl phenyl sulfone 
• 30540-31-9 1-bromo-2,3-dimethyl-butane 

Relevant articles and documents

Synthetic routes to campesterol and dihydrobrassicasterol: A first reported synthesis of the key phytosterol dihydrobrassicasterol

Phytosterols are increasingly used as health supplements in functional foods and are associated with having both positive and negative effects on health. Given this disparity, an investigation of their full individual biological profile is imperative in order to assure food safety. This paper describes the de novo synthesis of pure phytosterols in multigram scale and we report the first synthesis of the key phytosterol dihydrobrassicasterol along with a comparison of routes to campesterol. A detailed spectroscopic analysis is included with full assignment of the 13C NMR spectroscopic data of both compounds, mixtures and their precursors leading to the potential use of NMR spectroscopy as a tool for analysis of these sterol mixtures.

A Convenient Synthesis of (22S)-22-Hydroxycampesterol and Some Related Steroids

As possible candidates for intermediates in brassinolide biosynthesis, (22S)-22-hydroxycampesterol 1 and its related new steroids 5-7 are conveniently synthesized by employing the Grignard reaction of a known steroidal 22-aldehyde 8 with 2,3-dimethylbutylmagnesium bromide as a key reaction.