Details
Factory sells 2,4-Dimethyl-3-pentanol 600-36-2 with sufficient production capacity
- Molecular Formula: C7H16O
- Molecular Weight: 116.203
- Appearance/Colour: clear colorless liquid
- Vapor Pressure: 2.78mmHg at 25°C
- Melting Point: -70 °C
- Refractive Index: 1.425
- Boiling Point: 138.7 °C at 760 mmHg
- PKA: 15.04±0.20(Predicted)
- Flash Point: 37.2 °C
- PSA: 20.23000
- Density: 0.814 g/cm3
- LogP: 1.65930
2,4-Dimethyl-3-pentanol(Cas 600-36-2) Usage
|
Uses and Mechanism of Action |
2,4-Dimethyl-3-Pentanol is primarily utilized as a reductant in various catalytic processes, including Mo-catalyzed deoxygenation of epoxides to alkenes and Rhenium-catalyzed deoxydehydration of renewable biomass. In these catalytic reactions, 2,4-Dimethyl-3-pentanol acts as a sacrificial alcohol reductant, providing hydrogen atoms for the reduction of reactants, such as epoxides or vicinal diols, to yield desired products, such as alkenes. |
InChI:InChI=1/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3
600-36-2 Relevant articles
CATALYSIS WITH TRICARBONYL-tetrahapto-CYCLOPENTADIENONERUTHENIUM(0) COMPLEXES. A WATER-GAS TYPE REACTION
Shvo, Youval,Czarkie, Dorotha
, p. C25 - C28 (1986)
With water tricarbonyl-tetrahapto-tetrap...
Highly efficient NHC-iridium-catalyzed β-methylation of alcohols with methanol at low catalyst loadings
Lu, Zeye,Zheng, Qingshu,Zeng, Guangkuo,Kuang, Yunyan,Clark, James H.,Tu, Tao
, p. 1361 - 1366 (2021/06/30)
The methylation of alcohols is of great ...
A Practical and Stereoselective In Situ NHC-Cobalt Catalytic System for Hydrogenation of Ketones and Aldehydes
Zhong, Rui,Wei, Zeyuan,Zhang, Wei,Liu, Shun,Liu, Qiang
supporting information, p. 1552 - 1566 (2019/06/14)
Homogeneous catalytic hydrogenation of c...
Transfer Hydrogenation of Carbonyl Groups, Imines and N-Heterocycles Catalyzed by Simple, Bipyridine-Based MnI Complexes
Dubey, Abhishek,Rahaman, S. M. Wahidur,Fayzullin, Robert R.,Khusnutdinova, Julia R.
, p. 3844 - 3852 (2019/04/08)
Utilization of hydroxy-substituted bipyr...
Chemoselective Oxidation of Equatorial Alcohols with N-Ligated λ3-Iodanes
Mikhael, Myriam,Adler, Sophia A.,Wengryniuk, Sarah E.
supporting information, p. 5889 - 5893 (2019/08/26)
The site-selective and chemoselective fu...
600-36-2 Process route
-
-
67-56-1
methanol
-
-
142-68-7
TETRAHYDROPYRANE
-
-
10141-72-7
2-methyloxane
-
-
3857-14-5
2-ethyltetrahydropyran
-
-
4676-74-8
2-butyltetrahydropyran
-
-
110-62-3
pentanal
-
-
64-17-5
ethanol
-
-
2177-77-7
methyl 2-methylpentanoate
-
-
115-10-6,157621-61-9
Dimethyl ether
-
-
78-83-1
2-methyl-propan-1-ol
-
-
600-36-2
2,4-dimethyl-3-pentanol
-
-
107-31-3
Methyl formate
-
-
547-63-7,133320-07-7,67505-84-4
Methyl isobutyrate
-
-
623-42-7
butanoic acid methyl ester
-
-
624-24-8
methyl valerate
-
-
18641-70-8
2,4-Dimethyl-3-pentanone
-
-
626-33-5
2-methyl-4-heptanone
-
-
23936-98-3
2,4,5-trimethyl-hexan-3-one
-
-
19549-84-9
3-butyl ketone
-
-
502-56-7
nonanone-5
-
-
1528-25-2
3-ethylheptan-4-one
-
-
75-07-0,9002-91-9
acetaldehyde
-
-
123-38-6
propionaldehyde
-
-
110-13-4
2,5-hexanedione
-
-
78-84-2
isobutyraldehyde
-
-
565-80-0
2,4-dimethylpentan-3-one
| Conditions | Yield |
|---|---|
|
Cu-Zn-Mg-Al based catalyst; hydrogen reduced;
at 249.84 ℃;
Product distribution / selectivity;
|
-
-
185566-86-3
1-(1-Isopropyl-2-methyl-propoxy)-1-oxo-1H-1λ5 -benzo[d][1,2]iodoxol-3-one
-
-
600-36-2
2,4-dimethyl-3-pentanol
-
-
61717-82-6
1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione
| Conditions | Yield |
|---|---|
|
With
water;
In
dimethylsulfoxide-d6;
Equilibrium constant;
|
600-36-2 Upstream products
-
558-30-5
2-methyl-1,2-epoxypropane
-
920-39-8
isopropylmagnesium bromide
-
4390-75-4
2-hydroxy-2-isopropyl-3-methyl-butyronitrile
-
927-77-5
n-propylmagnesium bromide
600-36-2 Downstream products
-
34557-54-5
methane
-
617-94-7
1-methyl-1-phenylethyl alcohol
-
98-86-2
acetophenone
-
3623-52-7
isomenthol
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