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Buy Quality 2,6-dimethylhept-5-ene-1-nitrile 54088-65-2 In Stock with Immediately Delivery
- Molecular Formula: C9H15N
- Molecular Weight: 137.225
- Vapor Pressure: 0.183mmHg at 25°C
- Refractive Index: 1.442
- Boiling Point: 211.4 °C at 760 mmHg
- Flash Point: 87.9 °C
- PSA： 23.79000
- Density: 0.835 g/cm3
- LogP: 2.89248
2,6-dimethylhept-5-ene-1-nitrile(Cas 54088-65-2) Usage
|
Synonym |
DMH-N |
|
Type of compound |
Nitrile |
|
Cyano functional group |
-C≡N |
|
Physical state |
Colorless liquid |
|
Odor |
Faint, sweet, and fruity |
|
Solubility |
Insoluble in water, soluble in organic solvents |
|
Primary use |
Intermediate in the synthesis of other chemical compounds |
|
Secondary use |
Flavoring agent in the food industry |
|
Potential applications |
Manufacturing of pharmaceuticals and agricultural chemicals |
|
Safety precautions |
Potential irritant to skin, eyes, and respiratory system |
|
General Description |
2,6-dimethylhept-5-ene-1-nitrile, also known as DMH-N, is a chemical compound with the molecular formula C9H15N. It is a nitrile, which is a group of organic compounds containing a cyano functional group (-C≡N). DMH-N is a colorless liquid with a faint, sweet, and fruity odor, and it is insoluble in water but soluble in organic solvents. It is primarily used as an intermediate in the synthesis of other chemical compounds and is also used as a flavoring agent in the food industry. Additionally, it has potential applications in the manufacturing of pharmaceuticals and agricultural chemicals. However, it should be handled with care as it is a potential irritant to the skin, eyes, and respiratory system. |
InChI:InChI=1/C9H15N/c1-8(2)5-4-6-9(3)7-10/h5,9H,4,6H2,1-3H3
54088-65-2 Relevant articles
Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach
Betke, Tobias,Rommelmann, Philipp,Oike, Keiko,Asano, Yasuhisa,Gr?ger, Harald
supporting information, p. 12361 - 12366 (2017/09/06)
A cyanide-free platform technology for t...
Photoinduced, Copper-Catalyzed Carbon-Carbon Bond Formation with Alkyl Electrophiles: Cyanation of Unactivated Secondary Alkyl Chlorides at Room Temperature
Ratani, Tanvi S.,Bachman, Shoshana,Fu, Gregory C.,Peters, Jonas C.
supporting information, p. 13902 - 13907 (2016/01/15)
We have recently reported that, in the p...
Efficient dehydration of aldoximes to nitriles with TiCl3(OTf)
Iranpoor,Zeynizadeh
, p. 2747 - 2752 (2007/10/03)
Aromatic, alicyclic, olefinic as well as...
An elimination reaction of N-carbomethoxy-N,N-dimethylhydrazonium salts to alkyl nitriles
Xiao, Zejun,Timberlake, Jack W.
, p. 12715 - 12720 (2007/10/03)
A new kind of elimination of hydrazonium...
54088-65-2 Process route
-
-
80325-37-7
(+/-)-6-chloro-2-methyl-2-heptene
-
-
10442-39-4
tetra-n-butylammonium cyanide
-
-
54088-65-2
rac-2,6-dimethylhept-5-enenitrile
| Conditions | Yield |
|---|---|
|
With
copper(l) iodide;
In
acetonitrile;
at 20 ℃;
for 24h;
Inert atmosphere;
UV-irradiation;
|
85%
|
-
-
rac-2,6-dimethylhept-5-enaldehyde oxime
-
-
54088-65-2
rac-2,6-dimethylhept-5-enenitrile
| Conditions | Yield |
|---|---|
|
With
trichloro(trifluoromethanesulfonato)titanium(IV);
at 80 ℃;
for 10h;
|
94%
|
|
With
copper diacetate;
In
acetonitrile;
for 3h;
Reflux;
|
49%
|
54088-65-2 Upstream products
-
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-
4630-06-2
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-
143-33-9
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-
2270-59-9
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-
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-
18069-17-5
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-
67-64-1
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-
3792-53-8
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