(+)-trans-(R)-allethrin

Base Information

Chemical Name:(+)-trans-(R)-allethrin
CAS No.:61009-26-5
Molecular Formula:C₁₉H₂₆O₃
Molecular Weight:302.414
Hs Code.:
DSSTox Substance ID:DTXSID90897729
Nikkaji Number:J411.245H
Wikidata:Q27118148
Metabolomics Workbench ID:28038

Synonyms:(+)-trans-(R)-allethrin;(1R)-2-methyl-4-oxo-3-(prop-2-en-1-yl)cyclopent-2-en-1-yl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate;(1R)-3-allyl-2-methyl-4-oxocyclopent-2-en-1-yl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate;61009-26-5;Exrin;SCHEMBL8648414;CHEBI:39119;DTXSID90897729;LMPR0102060008;[(1R)-2-methyl-4-oxo-3-prop-2-enylcyclopent-2-en-1-yl] (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;Q27118148;(1R)-2,2-Dimethyl-3alpha-(2-methyl-1-propenyl)cyclopropane-1beta-carboxylic acid (R)-1-methyl-2-allyl-3-oxocyclopentene-5-yl ester;Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-, (1R)-2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl ester, (1R,3R)-

Suppliers and Price of (+)-trans-(R)-allethrin

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+)-trans-(R)-allethrin

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:302.18819469
Heavy Atom Count:22
Complexity:574

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C)CC=C
Isomeric SMILES:CC1=C(C(=O)C[C@H]1OC(=O)[C@@H]2[C@H](C2(C)C)C=C(C)C)CC=C

Technology Process of (+)-trans-(R)-allethrin

There total 14 articles about (+)-trans-(R)-allethrin 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: 85.0%