Bulk supply high purity (4alpha,4abeta,8aalpha)-octahydro-4,8a-dimethyl-4a(2H)-naphthol 5173-69-3, Paid sample available
- Molecular Formula: C12H22O
- Molecular Weight: 182.306
- Boiling Point: 252.4±8.0 °C(Predicted)
- PKA: 15.23±0.60(Predicted)
- PSA： 20.23000
- Density: 0.985±0.06 g/cm3(Predicted)
- LogP: 3.11780
(4alpha,4abeta,8aalpha)-octahydro-4,8a-dimethyl-4a(2H)-naphthol(Cas 5173-69-3) Usage
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General Description |
The chemical "(4alpha,4abeta,8aalpha)-octahydro-4,8a-dimethyl-4a(2H)-naphthol" is a bicyclic organic compound with a molecular formula C11H18O. It is a derivative of naphthol, containing a fused ring system and two methyl groups. (4alpha,4abeta,8aalpha)-octahydro-4,8a-dimethyl-4a(2H)-naphthol is primarily used in the synthesis of pharmaceuticals and agrochemicals. It may also have potential applications in fragrance and flavor industries. However, limited information is available about its specific properties and uses, and further research may be needed to fully understand its potential applications. |
InChI:InChI=1/C12H22O/c1-10-6-5-8-11(2)7-3-4-9-12(10,11)13/h10,13H,3-9H2,1-2H3/t10-,11-,12+/m0/s1
5173-69-3 Relevant articles
13. 1,2,3,4,4a,5,8,8a-Octahydro-4β,8aα-dimethylnaphthalen-4aβ-ol (=Dehydrogeosmin), a Novel Compound Occuring in the Flower Scent of Various Species of Cactaceae
Kaiser, Roman,Nussbaumer, Cornelius
, p. 133 - 139 (2007/10/02)
The 1,2,3,4,4a,5,8,8a-octahydro-4β,8aα-d...
Synthesis of (+/-)-Geosmin. Part 2. A One-Pot Four-Step Conversion of 1,4a-Dimethyl-1α,8aα-epoxyperhydronaphthalen-2-one into (+/-)-Geosmin
Hansson, Lars,Carlson, Rolf
, p. 1042 - 1045 (2007/10/02)
A one-pot four-step procedure for the co...
SYNTHESIS OF EARTHY-MOULDY SMELLING COMPOUNDS-I STEREOSELECTIVE SYNTHESIS OF (+/-)-GEOSMIN
Gosselin, P.,Joulain, D.,Laurin, P.,Rouessac, F.
, p. 2775 - 2778 (2007/10/02)
The strongly earthy-smelling compound (+...
Metabolites of bird's nest fungi. Part VI. The synthesis of (±)cybullol and a new synthesis of (±)geosmin
Ayer,Browne,Fung
, p. 3276 - 3282 (2007/10/11)
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5173-69-3 Process route
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![Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester](/upload/2026/4/fae5cccb75724dcaba3c900a23a7700d_33f3da86-5f4a-4b7d-8221-837c0410fc5c.png)
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125107-10-0,125137-16-8
Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester
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5173-69-3,5173-70-6,16423-19-1,16452-32-7,19700-21-1,23333-91-7,104873-46-3,132154-26-8
(+/-)-Geosmin
| Conditions | Yield |
|---|---|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
for 3h;
Heating;
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72%
|
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126370-56-7
(+/-)-perhydro-7β,8aβ-dihydroxy-1β-methylnaphthalene-4aα-carbaldehyde
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5173-69-3,5173-70-6,16423-19-1,16452-32-7,19700-21-1,23333-91-7,104873-46-3,132154-26-8
(+/-)-Geosmin
| Conditions | Yield |
|---|---|
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Multi-step reaction
with
4
steps
1: Py*TsOH / CH2
Cl2
/ 0.5 h / Ambient temperature
2: 1) N2
H4
; 2) KOH; 3) Py*TsOH / 1) 110 deg C, 30 min; 2) 180 deg C, 1 h; 3) MeOH, 60 deg C, 30 min
3: 90 percent / pyridine / CH2
Cl2
/ 24 h / Ambient temperature
4: Zn powder, NaI / 1,2-dimethoxy-ethane / 4 h / 90 - 95 °C
With
pyridine; potassium hydroxide; pyridinium p-toluenesulfonate; sodium iodide; hydrazine; zinc;
pyridinium p-toluenesulfonate;
In
1,2-dimethoxyethane; dichloromethane;
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5173-69-3 Upstream products
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16423-16-8
trans-8,10-Dimethyl-1(9) -octalin
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126370-59-0
Methanesulfonic acid (2S,4aR,8R,8aR)-8a-hydroxy-4a,8-dimethyl-decahydro-naphthalen-2-yl ester
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22249-39-4
1,4a-dimethyl-1α,8aα-epoxyperhydronaphthalen-2-one
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125107-10-0
Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester
5173-69-3 Downstream products
-
16423-16-8
markiertes 8ref,10cis-Dimethyl-1(9)-octalin
