6-METHYL-2-HEPTANOL
Contact usBuy cost-effective 99% pure 6-METHYL-2-HEPTANOL 4730-22-7 now
- Molecular Formula:C8H18 O
- Molecular Weight:130.23
- Vapor Pressure:0.342mmHg at 25°C
- Melting Point:-105°C
- Refractive Index:n20/D 1.424(lit.)
- Boiling Point:176°Cat760mmHg
- PKA:15.27±0.20(Predicted)
- Flash Point:67.2°C
- PSA:20.23000
- Density:0.819g/cm3
- LogP:2.19350
6-METHYL-2-HEPTANOL(Cas 4730-22-7) Usage
InChI:InChI=1/C8H18O/c1-7(2)5-4-6-8(3)9/h7-9H,4-6H2,1-3H3/t8-/m0/s1
4730-22-7 Relevant articles
Tuning Nano-Nickel Catalyst Hydrogenation Aptitude by On-the-Fly Zirconium Doping
Zienkiewicz-Machnik, Ma?gorzata,Goszewska, Ilona,Giziński, Damian,?r?bowata, Anna,Kuzmowicz, Katarzyna,Kubas, Adam,Matus, Krzysztof,Lisovytskiy, Dmytro,Pisarek, Marcin,Jacinto
, p. 3132 - 3138 (2020)
The effect of nano-Ni catalyst post-synt...
Base-free transfer hydrogenation of aryl-ketones, alkyl-ketones and alkenones catalyzed by an IrIIICp* complex bearing a triazenide ligand functionalized with pyrazole
Medrano-Castillo, Layla J.,Collazo-Flores, Miguel á.,Camarena-Díaz, Juan P.,Correa-Ayala, Erick,Chávez, Daniel,Grotjahn, Douglas B.,Rheingold, Arnold L.,Miranda-Soto, Valentín,Parra-Hake, Miguel
, (2020/03/13)
An IrIIICp* complex (2) bearing a triaze...
Rh(III)Cp? and Ir(III)Cp? Complexes of 1-[(4-Methyl)phenyl]-3-[(2-methyl-4′-R)imidazol-1-yl]triazenide (R = t-Bu or H): Synthesis, Structure, and Catalytic Activity
Camarena-Diáz, Juan P.,Iglesias, Ana L.,Chávez, Daniel,Aguirre, Gerardo,Grotjahn, Douglas B.,Rheingold, Arnold L.,Parra-Hake, Miguel,Miranda-Soto, Valentín
, p. 844 - 851 (2019/02/19)
A series of iridium and rhodium complexe...
STABILIZATION OF ACTIVE METAL CATALYSTS AT METAL-ORGANIC FRAMEWORK NODES FOR HIGHLY EFFICIENT ORGANIC TRANSFORMATIONS
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Paragraph 0338, (2019/01/07)
Metal-organic framework (MOFs) compositi...
4730-22-7 Process route
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110-93-0,129085-68-3
6-Methyl-hept-5-en-2-on
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-
4730-22-7
6-methyl-2-heptanol
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4630-06-2,1569-60-4
6-methylhept-5-en-2-ol
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928-68-7
6-methylheptan-2-one
| Conditions | Yield |
|---|---|
|
With
hydrogen;
Nic(w);
In
ethanol;
at 25 ℃;
for 11h;
under 760 Torr;
|
20 % Chromat. 15 % Chromat. 50 % Chromat. |
|
With
C34H28Cl2N3OPRu; potassium isopropoxide; isopropyl alcohol;
at 82 ℃;
for 2h;
under 750.075 Torr;
chemoselective reaction;
Inert atmosphere;
Schlenk technique;
|
58 %Chromat. |
|
With
hydrogen; sodium hydroxide;
In
methanol; water;
at 30 ℃;
for 40h;
under 30003 Torr;
Autoclave;
|
|
|
With
C25H35ClIrN5; potassium hydroxide;
In
isopropyl alcohol;
at 70 ℃;
for 38h;
Reagent/catalyst;
Overall yield = 96 %Spectr.;
|
|
|
With
C25H35ClN5Rh;
In
isopropyl alcohol;
at 70 ℃;
for 6h;
Overall yield = 95 %Spectr.;
|
-
-
110-93-0,129085-68-3
6-Methyl-hept-5-en-2-on
-
-
4730-22-7
6-methyl-2-heptanol
-
-
928-68-7
6-methylheptan-2-one
| Conditions | Yield |
|---|---|
|
With
[Ir(1-(1′-methylpyrazole)-3-(4′-methylphenyl)triazenide)Cp*Cl]; isopropyl alcohol;
at 90 ℃;
for 23h;
Time;
Overall yield = 100 percent;
Catalytic behavior;
Inert atmosphere;
Glovebox;
|
87% 13% |
|
With
hydrogen;
|
7.4% 19.6% |
|
With
bis[1-butyl-2-(diphenylphosphanyl)-3-methylimidazolium]tetrachloridoruthenium(III) hexafluorophosphate; potassium tert-butylate; isopropyl alcohol;
at 100 ℃;
for 2h;
Inert atmosphere;
Autoclave;
|
|
|
With
hydrogen; sodium hydroxide;
In
methanol; water;
at 30 ℃;
for 40h;
under 30003 Torr;
Reagent/catalyst;
Autoclave;
|
|
|
With
C25H35ClIrN5;
In
isopropyl alcohol;
at 70 ℃;
for 6h;
Reagent/catalyst;
Overall yield = 100 %Spectr.;
|
|
|
With
water;
In
ethanol;
at 65 ℃;
for 5h;
under 45004.5 Torr;
Reagent/catalyst;
Pressure;
Temperature;
Flow reactor;
|
4730-22-7 Upstream products
-
4630-06-2
6-methylhept-5-en-2-ol
-
110-93-0
6-Methyl-hept-5-en-2-on
-
2009-74-7
6-methyl-3-hepten-2-one
-
84912-18-5
2,5,9-trimethyl-dec-8-en-5-ol
4730-22-7 Downstream products
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4730-24-9
2-bromo-6-methyl-heptane
-
2350-19-8
6-Chlor-2-methyl-heptan
-
928-68-7
6-methylheptan-2-one
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102736-18-5
1,5-dimethylhexyl tosylate
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