ETHYL-O-TOLYL KETONE
- CasNo:2040-14-4
Product Description
Offer Chemical Raw Material ETHYL-O-TOLYL KETONE 2040-14-4 In Stock
- Molecular Formula: C10H12O
- Molecular Weight: 148.205
- Vapor Pressure: 0.119mmHg at 25°C
- Melting Point: -27.6°C
- Refractive Index: 1.506
- Boiling Point: 219.5 °C at 760 mmHg
- Flash Point: 93.8 °C
- PSA： 17.07000
- Density: 0.963 g/cm3
- LogP: 2.58770
ETHYL-O-TOLYL KETONE(Cas 2040-14-4) Usage
|
General Description |
Ethyl-O-Tolyl Ketone, also known as Ethylphenylketone or 1-phenyl-1-ethanone, is a chemical compound often used in the production of pharmaceuticals, perfumes, and other organic compounds. It has a strong, sweet, nutty aroma, making it a key compound in the fragrance industry. This chemical is known for its high reactivity, frequently used as an intermediate reagent in organic synthesis. Its molecular formula is C9H10O. Due to its reactivity, it needs to be handled with care, as it can cause eye irritation and skin allergies. Despite these potential hazards, it is not considered extremely dangerous or environmentally harmful. |
InChI:InChI=1/C10H12O/c1-3-10(11)9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3
2040-14-4 Relevant articles
Atom efficient Friedel-Crafts acylation of toluene with propionic anhydride over solid mesoporous superacid UDCaT-5
Yadav, Ganapati D.,Kamble, Shashikant B.
, p. 265 - 274 (2012)
Friedel-Crafts acylation is ubiquitous i...
KOtBu/DMSO Catalytic System for Isomerization of Allylic Alcohols to Ketones
Sai, Masahiro
supporting information, (2022/04/03)
The isomerization of allylic alcohols is...
Photoredox/nickel-catalyzed hydroacylation of ethylene with aromatic acids
Chen, Shuai,He, Hengchi,Li, Weipeng,Xie, Jin,Zhang, Lili,Zhu, Chengjian
supporting information, p. 9064 - 9067 (2021/09/15)
We report a general, practical and scala...
Combination of organocatalytic oxidation of alcohols and organolithium chemistry (RLi) in aqueous media, at room temperature and under aerobic conditions
Elorriaga, David,García-álvarez, Joaquín,González-Sabín, Javier,Hevia, Eva,Morís, Francisco,Presa Soto, Alejandro,Ríos-Lombardía, Nicolás,Rodríguez-álvarez, María Jesús
supporting information, p. 8932 - 8935 (2020/08/17)
A tandem protocol to access tertiary alc...
Palladium-catalyzed room temperature acylative cross-coupling of activated amides with trialkylboranes
Shi, Weijia,Zou, Gang
, (2018/10/02)
A highly efficient acylative cross-coupl...
2040-14-4 Process route
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-
97-94-9
triethyl borane
-
-
N-methyl-N-tosyl-2-methylbenzamide
-
-
2040-14-4
2-methylpropiophenone
| Conditions | Yield |
|---|---|
|
With
[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate;
In
tetrahydrofuran; tert-butyl methyl ether;
at 20 ℃;
for 24h;
Inert atmosphere;
Schlenk technique;
|
72%
|
-
-
61017-92-3
1-(2-methylphenyl)-1-propanol
-
-
2040-14-4
2-methylpropiophenone
| Conditions | Yield |
|---|---|
|
With
jones reagent;
In
acetone;
at 20 - 30 ℃;
|
95%
|
|
With
Jones reagent;
In
isopropyl alcohol; acetone;
at 0 ℃;
for 2.5h;
Inert atmosphere;
|
93%
|
|
With
chromium(VI) oxide; sulfuric acid;
In
acetone;
for 2h;
|
79.2%
|
|
With
chromium(VI) oxide; sulfuric acid;
In
water; acetone;
at 10 ℃;
for 2h;
|
69%
|
|
With
indium(III) triflate; chloroamine-T;
In
acetonitrile;
for 3h;
Reflux;
Inert atmosphere;
|
50%
|
|
|
|
|
With
1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
ethyl acetate;
Reflux;
|
|
|
With
sodium hypochlorite; potassium dihydrogenphosphate; 2-azaadamantane N-oxyl;
In
water;
at 20 ℃;
for 1h;
pH=7.9;
|
2040-14-4 Upstream products
-
10467-10-4
ethylmagnesium iodide
-
529-19-1
2-Methylbenzonitrile
-
925-90-6
ethylmagnesium bromide
-
61017-92-3
1-(2-methylphenyl)-1-propanol
2040-14-4 Downstream products
-
2523-03-7
3-dimethylamino-2-methyl-1-o -tolyl-propan-1-one
-
1074-17-5
1-Methyl-2-propylbenzene
-
5337-93-9
4'-methylpropiophenone
-
40685-23-2
1-o -tolyl-propan-1-one semicarbazone