73046-16-9

Basic information

• Product Name: (1S)-(+)-3-BROMOCAMPHOR-10-SULFONIC ACID HYDRATE
• Synonyms: (1S)-(+)-3-BROMOCAMPHOR-10-SULFONIC ACID HYDRATE
• CAS NO: 73046-16-9
• Molecular Formula: C₁₃H₂₂
• Molecular Weight: 329.21
• Mol File: 73046-16-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 117-121 °C(lit.)
• Boiling Point: 219.6°Cat760mmHg
• Flash Point: 77.2°C
• Appearance: /
• Density: 0.875g/cm³
• Vapor Pressure: 0.175mmHg at 25°C
• Refractive Index: 1.487
• CAS DataBase Reference: (1S)-(+)-3-BROMOCAMPHOR-10-SULFONIC ACID HYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-(+)-3-BROMOCAMPHOR-10-SULFONIC ACID HYDRATE(73046-16-9)
• EPA Substance Registry System: (1S)-(+)-3-BROMOCAMPHOR-10-SULFONIC ACID HYDRATE(73046-16-9)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 3261 8/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 73046-16-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H22/c1-12(2,3)10-7-8-11(9-10)13(4,5)6/h7,9H,8H2,1-6H3

Upstream product

• 507-19-7 t-butyl bromide 
• 542-92-7 cyclopenta-1,3-diene 
• 2175-91-9 6,6'-dimethyl fulvene 
• 67-64-1 acetone 

Downstream Products

• 130248-64-5 1-[(E)-(2,4-di-tert-butyl-2,4-cyclopentadien-1-ylidene)methyl]-4-methoxybenzene 
• 80438-66-0 1-bromo-2,4-di-tert-butylbenzene 
• 80438-65-9 1-chloro-2,4-di-tert-butylbenzene 
• 65130-67-8 1,3-di-tert-butyl-4-fluorobenzene 

Relevant articles and documents

Rational Synthesis of Metallo-Cations Toward Redox- A nd Alkaline-Stable Metallo-Polyelectrolytes

Cations are crucial components in emerging functional polyelectrolytes for a myriad of applications. Rapid development in this area necessitates the exploration of new cations with advanced properties. Herein we describe a combination of computational and experimental design of cobaltocene metallo-cations that have distinct electronic and redox properties. One of the direct outcomes on the first synthesis of a complete set of cation derivatives is to discover highly stable cations, which are further integrated to construct metallo-polyelectrolytes as anion-exchange membranes in solid-state alkaline fuel cells. The device performance of these polyelectrolytes under highly basic and oxidative environments is competitive with many organo-polyelectrolytes.

Improved Preparation of Polyisopropyl- and -tert-butylcyclopentadienes

Phase transfer catalytic isopropylation or tert-butylation of cyclopentadiene yields 1-6 in efficient one-pot procedures.Powdered potassium hydroxide or solid sodium hydride are the prefered bases, Aliquat 336 or dibenzo-18-crown-6 are the PT catalysts. +"--"+ Phase Transfer Catalysis, Potassium Hydroxide, Sodium Hydride

Di-tert-butylcyclopentadiene and tri-tert-butylcyclopentadiene

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