2-Propoxyphenol
- CAS: 6280-96-2
- Purity: 99%
- Manufacturer supply top purity 2-Propoxyphenol 6280-96-2 with ISO standards
Manufacturer supply top purity 2-Propoxyphenol 6280-96-2 with ISO standards
- Molecular Formula: C9H12O2
- Molecular Weight: 152.193
- Appearance/Colour: white to beige crystal
- Vapor Pressure: 0.0486mmHg at 25°C
- Refractive Index: 1.52
- Boiling Point: 228.5 °C at 760 mmHg
- PKA: 9.72±0.30(Predicted)
- Flash Point: 97.2 °C
- PSA： 29.46000
- Density: 1.05 g/cm3
- LogP: 2.18100
2-Propoxyphenol(Cas 6280-96-2) Usage
|
General Description |
2-Propoxyphenol, also known as propofol, is a chemical compound commonly used as a general anesthetic. It is a white, crystalline substance with a slightly sweet odor and is typically administered intravenously to induce and maintain anesthesia during surgeries or medical procedures. 2-Propoxyphenol acts as a sedative and hypnotic agent, producing a rapid onset of anesthesia and a quick recovery time. It works by enhancing the effect of gamma-aminobutyric acid (GABA) in the brain, leading to its sedative and anesthetic effects. Additionally, it has antiemetic properties, which helps prevent nausea and vomiting after surgery. Despite its widespread use in medical settings, propofol also has the potential for abuse and can result in adverse effects such as respiratory depression, low blood pressure, and potential allergic reactions. |
InChI:InChI=1/C9H12O2/c1-2-7-11-9-6-4-3-5-8(9)10/h3-6,10H,2,7H2,1H3
6280-96-2 Relevant articles
Direct oxidation of the C(sp2)-C(sp3) bond from benzyltrimethylsilanes to phenols
Li, Wei,Gao, Guolin,Gao, Yuan,Yang, Chao,Xia, Wujiong
supporting information, p. 5291 - 5293 (2017/07/10)
A novel pathway for direct conversion of...
Asymmetric synthesis of O-protected acyloins using enoate reductases: Stereochemical control through protecting group modification
Winkler, Christoph K.,Stueckler, Clemens,Mueller, Nicole J.,Pressnitz, Desiree,Faber, Kurt
supporting information; experimental part, p. 6354 - 6358 (2011/02/24)
O-Protected cyclic acyloins were obtaine...
METHODS AND COMPOSITIONS FOR CONTROL OF CABBAGE LOOPER, Trichoplusia ni
-
Page/Page column 9, (2010/07/04)
The invention provides in part dialkoxyb...
Dialkoxybenzene and dialkoxyallylbenzene feeding and oviposition deterrents against the cabbage looper, trichoplusia ni: Potential insect behavior control agents
Akhtar, Yasmin,Yu, Yang,Isman, Murray B.,Plettner, Erika
scheme or table, p. 4983 - 4991 (2011/08/06)
The antifeedant, oviposition deterrent, ...
6280-96-2 Process route
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-
120-80-9,19481-10-8,37349-32-9
benzene-1,2-diol
-
-
107-08-4
1-iodo-propane
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-
6280-96-2
2-propoxyphenol
| Conditions | Yield |
|---|---|
|
benzene-1,2-diol;
With
potassium carbonate;
In
acetone;
at 20 ℃;
for 2h;
1-iodo-propane;
In
acetone;
Product distribution / selectivity;
Heating;
Reflux;
|
80%
|
-
-
1126-20-1
2-allyloxyphenol
-
-
6280-96-2
2-propoxyphenol
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
In
methanol;
at 20 ℃;
for 96h;
|
21%
|
|
With
palladium 10% on activated carbon; hydrogen;
In
tetrahydrofuran;
at 20 ℃;
under 760.051 Torr;
|
6280-96-2 Upstream products
-
10467-10-4
ethylmagnesium iodide
-
60-29-7
diethyl ether
-
95-47-6
o-xylene
-
29515-39-7
1-methoxy-2-n-propoxybenzene
6280-96-2 Downstream products
-
110943-74-3
4-hydroxy-3-propoxybenzaldehyde
-
222031-84-7
2-hydroxy-3-n-propoxybenzaldehyde
-
1005005-55-9
2-allyl-6-propoxy phenol
-
1005005-88-8
(1-allyloxy-2-propoxybenzene)
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