3,4-Dimethylpent-1-en-3-ol
- Name 3,4-Dimethylpent-1-en-3-ol
- CAS 40076-53-7
- Purity 99%
Product Details
Top quality factory supply 40076-53-7 3,4-Dimethylpent-1-en-3-ol at low price
- Molecular Formula: C7H14O
- Molecular Weight: 114.188
- Vapor Pressure: 6.96mmHg at 25°C
- Boiling Point: 121.5°C at 760 mmHg
- Flash Point: 27.6°C
- PSA： 20.23000
- Density: 0.832g/cm3
- LogP: 1.57940
3,4-Dimethylpent-1-en-3-ol(Cas 40076-53-7) Usage
InChI:InChI=1/C7H14O/c1-5-7(4,8)6(2)3/h5-6,8H,1H2,2-4H3
40076-53-7 Relevant articles
Stereospecific Asymmetric Synthesis of Tertiary Allylic Alcohol Derivatives by Catalytic [2,3]-Meisenheimer Rearrangements
Yu, Xin,Wannenmacher, Nick,Peters, René
supporting information, p. 10944 - 10948 (2020/05/04)
Chiral acyclic tertiary allylic alcohols...
11-Step Total Synthesis of Teleocidins B-1-B-4
Nakamura, Hugh,Yasui, Kosuke,Kanda, Yuzuru,Baran, Phil S.
supporting information, p. 1494 - 1497 (2019/01/26)
A unified and modular approach to the te...
An efficient DABCO-catalyzed Ireland-Claisen rearrangement of allylic acrylates
Li, Yunxia,Wang, Quanrui,Goeke, Andreas,Fráter, Georg
, p. 288 - 292 (2007/10/03)
A novel DABCO-catalyzed Ireland-Claisen ...
Catalytic hydromagnesiation of 2-alkylbutadienes
Viktorov,Zubritskii
, p. 1773 - 1785 (2007/10/03)
The effect of alkyl substituents in 2-al...
40076-53-7 Process route
-
-
1482-15-1
3,4-dimethylpent-1-yn-3-ol
-
-
40076-53-7
3,4-Dimethyl-1-penten-3-ol
| Conditions | Yield |
|---|---|
|
With
hydrogen;
Lindlar's catalyst;
In
cyclohexane;
for 24h;
|
93%
|
|
With
hydrogen;
Lindlar's catalyst;
In
cyclohexane;
for 24h;
|
93%
|
|
With
palladium on activated charcoal; Lindlar's catalyst;
Hydrogenation;
|
|
|
With
hydrogen;
Lindlar's catalyst;
|
-
-
563-80-4
3-methyl-butan-2-one
-
-
40076-53-7
3,4-Dimethyl-1-penten-3-ol
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: 40 percent / KOH / diethyl ether / 0 °C
2: 93 percent / H2
/ Lindlar catalyst / cyclohexane / 24 h
With
potassium hydroxide; hydrogen;
Lindlar's catalyst;
In
diethyl ether; cyclohexane;
1: Favorskii reaction;
|
|
|
Multi-step reaction
with
2
steps
1: 40 percent / KOH / diethyl ether
2: 93 percent / H2
/ Lindlar catalyst / cyclohexane / 24 h
With
potassium hydroxide; hydrogen;
Lindlar's catalyst;
In
diethyl ether; cyclohexane;
1: Addition / 2: Catalytic hydrogenation;
|
|
|
Multi-step reaction
with
2
steps
1: ammonia
2: palladium/calcium carbonate / Hydrogenation
With
palladium on activated charcoal; Lindlar's catalyst; ammonia;
|
|
|
|
40076-53-7 Upstream products
-
1482-15-1
3,4-dimethylpent-1-yn-3-ol
-
920-39-8
isopropylmagnesium bromide
-
78-94-4
methyl vinyl ketone
-
563-80-4
3-methyl-butan-2-one
40076-53-7 Downstream products
-
14145-47-2
3,4-dimethylpenta-1,3-diene
-
1113-56-0
2,3-dimethyl-1,3-pentadiene
-
5731-99-7
2-isopropyl-1,3-butadiene
