40577
(S)-1-Octen-3-ol
≥95% (sum of enantiomers, GC)
Sinônimo(s):
(S)-Matsutake alcohol
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About This Item
Fórmula empírica (Notação de Hill):
C8H16O
Número CAS:
Peso molecular:
128.21
Número MDL:
Código UNSPSC:
12352002
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
≥95% (sum of enantiomers, GC)
Formulário
liquid
pureza óptica
enantiomeric ratio: ≥99:1 (GC)
grupo funcional
hydroxyl
cadeia de caracteres SMILES
CCCCC[C@H](O)C=C
InChI
1S/C8H16O/c1-3-5-6-7-8(9)4-2/h4,8-9H,2-3,5-7H2,1H3/t8-/m1/s1
chave InChI
VSMOENVRRABVKN-MRVPVSSYSA-N
Aplicação
(S)-1-Octen-3-ol can be used:
- As an odorant in the study of an olfactory sensory map of the Anopheles gambiae maxillary palp.[1]
- As an intermediate in the synthesis of natural product polyporolide and a prostaglandin named 8-aza-prostaglandin E1.[2][3]
- As a substrate in the preparation of trienols by reacting with 1-iodo-1,3-dienes using Pd(OAc)2/AgOAc.[4]
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
154.4 °F - closed cup
Ponto de fulgor (°C)
68 °C - closed cup
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti.
Jonathan D Bohbot et al.
PloS one, 4(9), e7032-e7032 (2009-09-16)
Enantiomers differ only in the left or right handedness (chirality) of their orientations and exhibit identical chemical and physical properties. In chemical communication systems, enantiomers can be differentially active at the physiological and behavioral levels. Only recently were enantioselective odorant
Odor coding in the maxillary palp of the malaria vector mosquito Anopheles gambiae
Lu T, et al.
Current Biology, 17(18), 1533-1544 (2007)
A stereoselective synthesis of the reported structure of polyporolide
Patil PH and Fernandes RA
Royal Society of Chemistry Advances, 5(61), 49189-49194 (2015)
Damien Brandt et al.
Organic letters, 14(21), 5594-5597 (2012-10-24)
The stereoselective synthesis of conjugated trienes has been achieved from allylic alcohols and 1-iodo-1,3-dienes using Pd(OAc)(2)/AgOAc.
Alan J Grant et al.
PloS one, 6(6), e21785-e21785 (2011-07-09)
1-Octen-3-ol (octenol) is a common attractant released by vertebrates which in combination with carbon dioxide (CO(2)) attracts hematophagous arthropods including mosquitoes. A receptor neuron contained within basiconic sensilla on the maxillary palps of adult mosquitoes responds selectively to 1-octen-3-ol. Recently
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