Details
Buy high quality and low price O-TOLYL BENZOATE 617-02-7 now
- Molecular Formula: C14H12O2
- Molecular Weight: 212.248
- Vapor Pressure: 1.23E-05mmHg at 25°C
- Refractive Index: 1.5700
- Boiling Point: 368.9 °C at 760 mmHg
- Flash Point: 154.5 °C
- PSA： 26.30000
- Density: 1.122 g/cm3
- LogP: 3.21420
O-TOLYL BENZOATE(Cas 617-02-7) Usage
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General Description |
O-Tolyl benzoate is a chemical compound that consists of a benzene ring with a benzoate group attached to the para-position of the tolyl group. It is often used as a fragrance ingredient in perfumes and other scented products due to its pleasant and fruity odor. Additionally, o-tolyl benzoate is utilized as a plasticizer in the manufacturing of plastics and resins, where it helps to improve flexibility and durability of the materials. O-TOLYL BENZOATE also has potential pharmaceutical applications, as it exhibits anti-inflammatory and anti-cancer properties, making it a subject of interest for medicinal research. Overall, o-tolyl benzoate has diverse uses in various industries, from fragrance and plastics to potential therapeutic purposes. |
InChI:InChI=1/C14H12O2/c1-11-7-5-6-10-13(11)16-14(15)12-8-3-2-4-9-12/h2-10H,1H3
617-02-7 Relevant articles
Conversion of esters to thioesters under mild conditions
Shi, Yijun,Liu, Xuejing,Cao, Han,Bie, Fusheng,Han, Ying,Yan, Peng,Szostak, Roman,Szostak, Michal,Liu, Chengwei
supporting information, p. 2991 - 2996 (2021/04/14)
We report conversion of esters to thioes...
Hydrogen-bond-assisted transition-metal-free catalytic transformation of amides to esters
Huang, Changyu,Li, Jinpeng,Wang, Jiaquan,Zheng, Qingshu,Li, Zhenhua,Tu, Tao
, p. 66 - 71 (2020/11/18)
The amide C-N cleavage has drawn a broad...
Unexpected migration of a benzoyl group in the intramolecular Wittig reaction of o-acyloxybenzylidenephosphoranes with benzoyl chlorides: One-pot synthesis of isomeric 3-benzoyl-2-phenylbenzofurans
Begala, Michela,Mancinelli, Michele,Delogu, Giovanna Lucia
supporting information, (2020/01/28)
The reaction of o-acyloxybenzylidenetrip...
Supramolecular Pd(II) complex of DPPF and dithiolate: An efficient catalyst for amino and phenoxycarbonylation using Co2(CO)8 as sustainable C1 source
Gaikwad, Vinayak V.,Mane, Pravin A.,Dey, Sandip,Patel, Divya,Bhanage, Bhalchandra M.
, (2019/11/28)
Highly active, efficient and robust “dpp...
617-02-7 Process route
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614-45-9
tert-Butyl peroxybenzoate
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-
108-88-3,15644-74-3,16713-13-6
toluene
-
-
614-34-6
p-cresyl benzoate
-
-
617-02-7
2-methylphenyl benzoate
-
-
614-32-4
3-methylphenyl benzoate
-
-
120-51-4
benzoic acid benzyl ester
| Conditions | Yield |
|---|---|
|
dibenzoatopalladium(II);
In
acetic acid;
at 100 ℃;
for 3h;
Yield given. Yields of byproduct given;
|
-
-
6597-18-8
(dibenzoyloxyiodo)benzene
-
-
108-88-3,15644-74-3,16713-13-6
toluene
-
-
614-34-6
p-cresyl benzoate
-
-
617-02-7
2-methylphenyl benzoate
| Conditions | Yield |
|---|---|
|
With
2,4,6-trimethyl-pyridine; palladium(II) trifluoroacetate;
at 100 ℃;
for 4h;
Overall yield = 60 %Chromat.;
Sealed tube;
|
617-02-7 Upstream products
-
98-88-4
benzoyl chloride
-
95-48-7
ortho-cresol
-
2902-69-4
2,2,2-trichloroacetophenone
-
65-85-0
benzoic acid
617-02-7 Downstream products
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5326-42-1
3-methyl-4-hydroxybenzophenone
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73374-11-5
benzoate de bromomethyl-2 phenyle
-
52727-93-2
benzoic acid-(4-bromo-2-methyl-phenyl ester)
-
102242-31-9
4-hydroxy-3-methylbenzophenone benzoate
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