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2-Methyl-1,2,3,4-diepoxybutane

Base Information
  • Chemical Name:2-Methyl-1,2,3,4-diepoxybutane
  • CAS No.:6341-85-1
  • Molecular Formula:C5H8O2
  • Molecular Weight:100.117
  • Hs Code.:2910900090
  • NSC Number:48599
  • DSSTox Substance ID:DTXSID90979594
  • Nikkaji Number:J70.052E
  • Mol file:6341-85-1.mol
2-Methyl-1,2,3,4-diepoxybutane

Synonyms:2-Methyl-1,2,3,4-diepoxybutane;2-Methyl-2,2'-bioxirane;6341-85-1;2-methyl-2-(oxiran-2-yl)oxirane;1,2,3,4-Diepoxy-2-methylbutane;2,2'-Bioxirane, 2-methyl-;CCRIS 5688;NSC 48599;BRN 0103138;BUTANE, 1,2:3,4-DIEPOXY-2-METHYL-;NSC48599;SCHEMBL3133959;DTXSID90979594;Butane,2:3,4-diepoxy-2-methyl-;NSC-48599;AKOS006279040;2,2'-Bioxirane, 2-methyl- (9CI);LS-45692;EN300-7577123

Suppliers and Price of 2-Methyl-1,2,3,4-diepoxybutane
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 2-METHYL-1,2,3,4-DIEPOXYBUTANE 95.00%
  • 5MG
  • $ 504.71
Total 8 raw suppliers
Chemical Property of 2-Methyl-1,2,3,4-diepoxybutane
Chemical Property:
  • Refractive Index:1.4043 (estimate) 
  • Boiling Point:185°C (estimate) 
  • Flash Point:41.7oC 
  • PSA:25.06000 
  • Density:0.9971 (rough estimate) 
  • LogP:0.17410 
  • XLogP3:-0.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:100.052429494
  • Heavy Atom Count:7
  • Complexity:102
Purity/Quality:

2-METHYL-1,2,3,4-DIEPOXYBUTANE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Plastics & Rubber -> Epoxides
  • Canonical SMILES:CC1(CO1)C2CO2
Technology Process of 2-Methyl-1,2,3,4-diepoxybutane

There total 3 articles about 2-Methyl-1,2,3,4-diepoxybutane 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:
Guidance literature:
With dihydrogen peroxide; sodium oxalate; manganese triacetate; oxalic acid; N,N',N''-trimethyl-1,4,7-triazacyclononane; In water; acetonitrile; at -40 - 25 ℃; for 8.5 - 12h; under 2400.24 - 3900.39 Torr; Product distribution / selectivity;
Guidance literature:
With 1,1,1-trichloro-2,3-epoxypropane; NADPH-generating system; rat liver microsomal proteins; In phosphate buffer; for 1h; Further Variations:; Reagents; Enzyme kinetics;
DOI:10.1021/tx000061a
Guidance literature:
DOI:10.1021/jo01065a629
upstream raw materials:

isoprene

isoprene epoxide

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