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[1R-(1alpha,2alpha,5alpha)]-5-(isopropyl)-2-methylcyclohexan-1-ol
- Name [1R-(1alpha,2alpha,5alpha)]-5-(isopropyl)-2-methylcyclohexan-1-ol
- CAS 3858-45-5
- Purity 99%
Product Details
Manufacturer supply top purity [1R-(1alpha,2alpha,5alpha)]-5-(isopropyl)-2-methylcyclohexan-1-ol 3858-45-5 with ISO standards
- Molecular Formula: C10H20 O
- Molecular Weight: 156.268
- Boiling Point: 222°Cat760mmHg
- Flash Point: 86.7°C
- PSA： 20.23000
- Density: 0.89g/cm3
- LogP: 2.43950
[1R-(1alpha,2alpha,5alpha)]-5-(isopropyl)-2-methylcyclohexan-1-ol(Cas 3858-45-5) Usage
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General Description |
The chemical "[1R-(1alpha,2alpha,5alpha)]-5-(isopropyl)-2-mmethylcyclohexan-1-ol" is a specific isomer of a cyclohexanol compound with a molecular formula of C10H20O. It is a colorless liquid with a strong, minty odor. This chemical is commonly used in the manufacture of perfumes and other scented products due to its pleasant odor. It also has potential applications in the production of pharmaceuticals and as a flavoring agent in food products. Furthermore, it can be used as a solvent in various industrial processes. This chemical is important because of its versatile uses across different industries. |
InChI:InChI=1/C10H20O/c1-7(2)9-5-4-8(3)10(11)6-9/h7-11H,4-6H2,1-3H3
3858-45-5 Relevant articles
Simple H2-free hydrogenation of unsaturated monoterpenoids catalyzed by Raney nickel
Philippov, Alexey A.,Chibiryaev, Andrey M.,Martyanov, Oleg N.
, p. 380 - 381 (2019/08/20)
A series of monoterpenoids (citral, carv...
P450-catalyzed regio- and stereoselective oxidative hydroxylation of disubstituted cyclohexanes: Creation of three centers of chirality in a single CH-activation event This paper is dedicated to the memory of Harry H. Wasserman
Ilie, Adriana,Agudo, Rubén,Roiban, Gheorghe-Doru,Reetz, Manfred T.
, p. 470 - 475 (2015/02/02)
Wild-type P450-BM3 is able to catalyze i...
Radical chain reduction of alkylboron compounds with catechols
Villa, Giorgio,Povie, Guillaume,Renaud, Philippe
supporting information; experimental part, p. 5913 - 5920 (2011/06/16)
The conversion of alkylboranes to the co...
Reduction of α, β-unsaturated ketones using a Zn/NiCl 2 system in aqueous media in the presence of anionic and cationic surfactants
Ilikti, Hocine,Benabdallah, Tayeb,Bentayeb, Kamel,Othman, Adil A.,Derriche, Zoubir
, p. 31 - 36 (2008/12/22)
The reduction of aromatic and aliphatic ...
3858-45-5 Process route
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-
1678-82-6
trans-1,4-menthane
-
-
498-81-7
p-menthan-8-ol
-
-
499-69-4,1126-39-2,1126-40-5,1126-41-6,1845-59-6,3127-80-8,3858-43-3,3858-45-5,3858-47-7,3858-49-9,5563-78-0,42846-32-2,116783-34-7,60320-28-7
(+/-)-menthol
-
-
3901-95-9
cis p-menthanol
-
-
470-65-5
p-menthane-4-ol
-
-
490-99-3,491-01-0,491-02-1,1490-04-6,2216-51-5,2216-52-6,3623-51-6,3623-52-7,3623-53-8,15356-60-2,15356-70-4,20747-49-3,20752-33-4,20752-34-5,23283-97-8,64282-88-8,89-78-1
DL-neomenthol
| Conditions | Yield |
|---|---|
|
With
monooxygenase P450-BM3; nicotinamide adenine dinucleotide phosphate;
for 3h;
stereoselective reaction;
Catalytic behavior;
Enzymatic reaction;
|
-
-
499-75-2
carvacrol
-
-
499-69-4,1126-39-2,1126-40-5,1126-41-6,1845-59-6,3127-80-8,3858-43-3,3858-45-5,3858-47-7,3858-49-9,5563-78-0,42846-32-2,116783-34-7,60320-28-7
(+/-)-menthol
| Conditions | Yield |
|---|---|
|
With
hydrogen;
platinum;
at 170 ℃;
for 6h;
under 2400.24 Torr;
|
85%
|
3858-45-5 Upstream products
-
2244-16-8
(S)-p-mentha-6,8-dien-2-one
-
99-49-0
Carvone
-
64-17-5
ethanol
-
43205-82-9
carvotanacetone
