34956-85-9

Basic information

• Product Name: 2-(5-bromopentyl)-2-ethyl-1,3-dioxolane
• CAS NO: 34956-85-9
• Molecular Formula: C₁₀H₁₉BrO₂
• Molecular Weight: 251.1607
• Mol File: 34956-85-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 278°C at 760 mmHg
• Flash Point: 116.6°C
• Density: 1.212g/cm³
• Vapor Pressure: 0.00737mmHg at 25°C
• Refractive Index: 1.464
• CAS DataBase Reference: 2-(5-bromopentyl)-2-ethyl-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-bromopentyl)-2-ethyl-1,3-dioxolane(34956-85-9)
• EPA Substance Registry System: 2-(5-bromopentyl)-2-ethyl-1,3-dioxolane(34956-85-9)

Safety Data

• Hazardous Substances Data: 34956-85-9(Hazardous Substances Data)

Usage

General Description

2-(5-bromopentyl)-2-ethyl-1,3-dioxolane is a chemical compound with the molecular formula C9H17BrO2. It is a colorless liquid with a sweet, fruity odor. This chemical is used in the production of pharmaceuticals and as a solvent in various industrial processes. It is also used as a reagent in organic synthesis and in the manufacturing of flavors and fragrances. 2-(5-bromopentyl)-2-ethyl-1,3-dioxolane is known to be flammable and should be handled with care in a well-ventilated area. Its precise properties and applications are dependent on its specific formulation and purity.

Upstream product

• 2146-62-5 8-bromo-octan-3-one 
• 107-21-1 ethylene glycol 
• 6621-59-6 6-bromo-1-hexanenitrile 
• 1940-18-7 1-ethylcyclohexanol 

Downstream Products

• 635680-16-9 2-amino-8-oxo-decanoic acid methyl ester 
• 891269-98-0 6-(2-Ethyl-1,3-dioxolan-2-yl)-1-(2-phenyl-1,3-thiazol-5-yl)hexan-1-one 
• 891269-79-7 6-(2-Ethyl-1,3-dioxolan-2-yl)-1-(4-phenyl-2-thienyl)hexan-1-ol 

Relevant articles and documents

Efficient Syntheses of Biologically Important (S)-2-Amino-8-oxodecanoic Acid (Aoda) and Homologues

The efficient and practical asymmetric syntheses of the biologically important (S)-2-amino-8-oxodecanoic ester and its homologues have been achieved employing the Schoellkopf chiral auxiliary. Carbon-carbon bond formation between the appropriate alkyl bromide and the LDA generated anion of the Schoellkopf auxiliary, followed by hydrolysis provided the desired methyl ester of a long-chained keto amino acid in high yield with high selectivity.

Ring-closing metathesis in the synthesis of biologically active peptidomimetics of apicidin A

Syntheses of novel 16-membered macrocyclic peptidomimetics are reported, which employ iterative peptide coupling followed by high yielding ring-closing metathesis (RCM) as the key cyclization step. The target macrocyclic compounds include examples contain