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Limonene oxide, cis-(-)-

Base Information Edit
  • Chemical Name:Limonene oxide, cis-(-)-
  • CAS No.:32543-51-4
  • Molecular Formula:C10H16O
  • Molecular Weight:152.236
  • Hs Code.:
  • UNII:215X25J847
  • DSSTox Substance ID:DTXSID80186250
  • Nikkaji Number:J350.264C
  • Wikidata:Q27253522
  • Mol file:32543-51-4.mol
Limonene oxide, cis-(-)-

Synonyms:Limonene oxide, cis-(-)-;32543-51-4;cis-(-)-limonene oxide;cis-(-)-1,2-Epoxy-p-menth-8-ene;FEMA No. 4656, cis-(-)-;(1S,4S,6R)-1-Methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane;UNII-215X25J847;215X25J847;7-Oxabicyclo(4.1.0)heptane, 1-methyl-4-(1-methylethenyl)-, (1S,4S,6R)-;7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(1-methylethenyl)-, (1S,4S,6R)-;7-Oxabicyclo(4.1.0)heptane, 1-methyl-4-(1-methylethenyl)-, (1S-(1alpha,4alpha,6alpha))-;-(-) limonene oxide;SCHEMBL230827;cis-(?)-Limonene-1,2-epoxide;DTXSID80186250;7-OXABICYCLO(4.1.0)HEPTANE, 1-METHYL-4-(1-METHYLETHENYL)-, (1S-(1.ALPHA.,4.ALPHA.,6.ALPHA.))-;AT23319;(-)-(1S,4S)-limonene-1,2- epoxide;Q27253522;(1S,4S,6R)-1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane;GHI

Suppliers and Price of Limonene oxide, cis-(-)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 0 raw suppliers
Chemical Property of Limonene oxide, cis-(-)- Edit
Chemical Property:
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:152.120115130
  • Heavy Atom Count:11
  • Complexity:197
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=C)C1CCC2(C(C1)O2)C
  • Isomeric SMILES:CC(=C)[C@H]1CC[C@]2([C@@H](C1)O2)C
Technology Process of Limonene oxide, cis-(-)-

There total 36 articles about Limonene oxide, cis-(-)- 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 limonene-1,2-epoxide hydrolase from Rhodococcus erythropolis; In aq. phosphate buffer; acetonitrile; at 20 ℃; for 2h; pH=8; Enzymatic reaction;
DOI:10.1002/cctc.201500608
Guidance literature:
With Fe(bpmen)(OTf)2; dihydrogen peroxide; acetic acid; In acetonitrile; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.tet.2013.02.013
Guidance literature:
With oxygen; isobutyraldehyde; [Ru(TAZS)(p-cymene)]2; In dichloromethane; at 20 ℃; for 8h; Further Variations:; Catalysts; Product distribution;
DOI:10.1016/S0040-4039(02)02072-5
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