2,3-epoxy-2-methylpentane

Base Information

• Chemical Name: 2,3-epoxy-2-methylpentane
• CAS No.: 1192-22-9
• Molecular Formula: C6H12 O
• Molecular Weight: 100.161
• Hs Code.: 2910900090
• DSSTox Substance ID: DTXSID30922887
• Nikkaji Number: J69.486J
• Mol file: 1192-22-9.mol

Synonyms:Pentane,2,3-epoxy-2-methyl- (7CI,8CI); 2,3-Epoxy-2-methylpentane;2-Ethyl-3,3-dimethyloxirane; 2-Methyl-2-pentene oxide; 3-Ethyl-2,2-dimethyloxirane

Chemical Property of 2,3-epoxy-2-methylpentane

Chemical Property:

• Vapor Pressure: 58.1mmHg at 25°C
• Refractive Index: 1.4800 (estimate)
• Boiling Point: 92.6°Cat760mmHg
• Flash Point: 4.3°C
• PSA: 12.53000
• Density: 0.832g/cm³
• LogP: 1.57380
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 100.088815002
• Heavy Atom Count: 7
• Complexity: 76.2

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,3-EPOXY-2-METHYLPENTANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1C(O1)(C)C
• Use Description: 2,3-Epoxy-2-methylpentane, also known as isobutyl vinyl ether, finds applications in various fields. In the chemical industry, it serves as a starting material for the synthesis of other compounds and can be used as a reactant in organic synthesis reactions. In the field of polymer chemistry, it can act as a comonomer in the production of certain polymers and copolymers, contributing to the development of specialized materials. Furthermore, it has applications in the realm of organic synthesis for creating pharmaceuticals, agrochemicals, and fine chemicals. Its versatility as a chemical building block makes it valuable across different sectors of the chemical and materials science industries, playing a pivotal role in the creation of various compounds and materials.

Technology Process of 2,3-epoxy-2-methylpentane

There total 13 articles about 2,3-epoxy-2-methylpentane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

2-methyl-2-pentene (625-27-4) → 2,3-epoxy-2-methylpentane (1192-22-9)

Guidance literature:

With 3,3-dimethyldioxirane; In acetone; at 23 ℃; Further Variations:; Solvents; Kinetics;

DOI:10.3390/90300117

Reference yield: 57.0%

2-methyl-2-pentene (625-27-4) + 1,1,3,3-tetrachloropropanone (632-21-3) → 2,3-epoxy-2-methylpentane (1192-22-9) + tetrachloroacetone hydrate (78950-58-0)

Guidance literature:

With disodium hydrogenphosphate; dihydrogen peroxide; In chloroform; for 24h; Ambient temperature;

DOI:10.1016/S0040-4039(01)93284-8

Reference yield:

2-methyl-2-pentene (625-27-4) → 2,3-epoxy-2-methylpentane (1192-22-9) + propionaldehyde (123-38-6) + acetone (67-64-1)

Guidance literature:

With (2-diethylaminocarbonylpyridine)2VO(O₂); In dichloromethane; at 20 ℃; for 2h; further reagents (pyridine-2-carboxylate)VO(O2)(H2O)2, <(pyridine-2-carboxylate)2VO(O2)>^-H⁺*H2O, <(pyridine-2-carboxylate)2VO(O2)>^-H⁺*HMPT, further solvent MeCN;

DOI:10.1021/ja00348a025

upstream raw materials:

2-methyl-2-pentene

1,1,3,3-tetrachloropropanone

1,3,2-dioxaphospholane

2-methylpentane-2,3-diol

Downstream raw materials:

2-methylpent-1-en-3-yl tert-butyldiphenylsilyl ether

2-Benzyloxy-2-methyl-pentan-3-ol

ethyl isopropyl ketone

(S)-(+)-3-methylpentan-2-one