Lilac aldehyde

Base Information

Chemical Name:Lilac aldehyde
CAS No.:81967-88-6
Molecular Formula:C10H16O2
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID90867402
Nikkaji Number:J501.066G
Wikidata:Q27109862
Mol file:81967-88-6.mol

Synonyms:Lilac aldehyde;2-(5-ethenyl-5-methyloxolan-2-yl)propanal;67920-63-2;Lilac aldehyde B;UNII-CZ348GQG4G;2-(5-Methyl-5-vinyltetrahydro-2-furanyl)propanal;2-(5-methyl-5-vinyltetrahydrofuran-2-yl)propanal;2-(5-ethenyl-5-methyltetrahydrofuran-2-yl)propanal;2-Furanacetaldehyde, 5-ethenyltetrahydro-alpha,5-dimethyl-;(+/-)-2-(5-Methyl-5-vinyltetrahydrofuran-2-yl)propionaldehyde;51685-39-3;(+/-)-lilac aldehyde;Lilac aldehyde (isomer II);CZ348GQG4G;SCHEMBL3505874;CHEBI:25038;DTXSID90867402;2-Furanacetaldehyde, 5-ethenyltetrahydro-.alpha.,5-dimethyl-, (.alpha.S,2S,5S)-;(+-)-2-(5-METHYL-5-VINYLTETRAHYDROFURAN-2-YL)PROPIONALDEHYDE;2-(5-Methyl-5-vinyltetrahydro-2-furanyl)propanal #;Q27109862;5-Ethenyltetrahydro-alpha,5-dimethyl-2-Furanacetaldehyde

Suppliers and Price of Lilac aldehyde

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

Total 3 raw suppliers

Chemical Property of Lilac aldehyde

Chemical Property:

Vapor Pressure:0.1mmHg at 25°C
Boiling Point:222.7°C at 760 mmHg
Flash Point:78.4°C
PSA：26.30000
Density:0.998g/cm³
LogP:1.94510
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:188

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C=O)C1CCC(O1)(C)C=C

Technology Process of Lilac aldehyde

There total 15 articles about Lilac aldehyde 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: 87.0%

: 118014-46-3
(+/-)-(E)-2,6-dimethyl-6-hydroxy-2,7-octadienal

: 51685-39-3,67920-63-2,81967-88-6
2-(5-ethenyl-5-methyloxolane-2-yl)propanal

Guidance literature:: With methanol; sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1016/S0031-9422(03)00142-0

Reference yield:

: 118014-46-3
(+/-)-(E)-2,6-dimethyl-6-hydroxy-2,7-octadienal

: 51685-39-3,67920-63-2,81967-88-6
2-(5-ethenyl-5-methyloxolane-2-yl)propanal

: 17015-30-4
2-methyl-6-methylene-2,7-octadienal

: 128463-66-1
2,6-dimethyl-2,5,7-octatrienal

Guidance literature:: With potassium hydrogensulfate; at 180 ℃; Title compound not separated from byproducts;
DOI:10.1021/jf00035a047

Reference yield:

: 61476-71-9
(R)-8-oxolinalool

: 51685-39-3,53447-45-3,53447-46-4,53447-47-5,53447-48-6,54809-54-0,54809-55-1,54809-56-2,54809-57-3,67920-63-2,81967-88-6
2-((5R)-5-methyl-5-vinyltetrahydrofuran-2-yl)propion aldehyde

: 526214-72-2
(2S)-2-((2S, 5R)-5-methyl-5-vinyltetrahydrofuran-2-yl)propion aldehyde

Guidance literature:: (R)-8-oxolinalool; With C₂₀H₂₇NOSi; In hexane; at 20 ℃; for 24h;

With hydrogenchloride; sodium hydrogencarbonate; In hexane; water; Overall yield = 27 %; Overall yield = 54.3 mg;
DOI:10.1055/s-0034-1380684