Home >Organic Chemicals > 3-ACETYLBENZONITRILE
- Chemical Name: 3-ACETYLBENZONITRILE
- CAS No.: 6136-68-1
Factory Sells Best Quality 3-ACETYLBENZONITRILE 6136-68-1 with stock
- Molecular Formula: C9H7NO
- Molecular Weight: 145.161
- Appearance/Colour: pale yellowish-orange to brown powder
- Melting Point: 98-100 °C(lit.)
- Refractive Index: 1.654
- Boiling Point: 267.3 °C at 760 mmHg
- Flash Point: 115.5 °C
- PSA: 40.86000
- Density: 1.11 g/cm3
- LogP: 1.76088
3-ACETYLBENZONITRILE(Cas 6136-68-1) Usage
InChI:InChI=1/C26H23Cl2N3O2S/c1-17-4-2-6-21(14-17)29-25(33)23-16-24(32)31(13-12-18-8-10-19(27)11-9-18)26(34-23)30-22-7-3-5-20(28)15-22/h2-11,14-15,23H,12-13,16H2,1H3,(H,29,33)/b30-26-
6136-68-1 Relevant articles
Photoinduced Acetylation of Anilines under Aqueous and Catalyst-Free Conditions
Yang, Yu-Ming,Yan, Wei,Hu, Han-Wei,Luo, Yimin,Tang, Zhen-Yu,Luo, Zhuangzhu
, p. 12344 - 12353 (2021/09/02)
A green and efficient visible-light indu...
Nickel-Catalyzed Reversible Functional Group Metathesis between Aryl Nitriles and Aryl Thioethers
Delcaillau, Tristan,Boehm, Philip,Morandi, Bill
supporting information, p. 3723 - 3728 (2021/04/07)
We describe a new functional group metat...
Synthesis method of aromatic benzyl ketone
-
Paragraph 0056-0061, (2020/09/12)
The invention discloses a synthesis meth...
Selective Synthesis of Secondary and Tertiary Amines by Reductive N-Alkylation of Nitriles and N-Alkylation of Amines and Ammonium Formate Catalyzed by Ruthenium Complex
Alshakova, Iryna D.,Nikonov, Georgii I.
, p. 5370 - 5378 (2019/06/14)
A new ruthenium catalytic system for the...
6136-68-1 Process route
-
-
41908-11-6
3-acetylbenzaldehyde
-
-
6136-68-1
3-acethylbenzonitrile
| Conditions | Yield |
|---|---|
|
With
hydroxylamine hydrochloride;
In
glycerol;
at 90 ℃;
for 8h;
Green chemistry;
|
83%
|
|
With
O-(diphenylphosphinyl)hydroxylamine;
In
toluene;
at 20 - 85 ℃;
chemoselective reaction;
|
75%
|
-
-
potassiumhexacyanoferrate(II) trihydrate
-
-
2142-63-4
1-(3-Bromophenyl)ethanone
-
-
6136-68-1
3-acethylbenzonitrile
| Conditions | Yield |
|---|---|
|
With
tetrakis(triphenylphosphine) palladium(0); 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
water; tert-butyl alcohol;
at 85 ℃;
for 16h;
Inert atmosphere;
|
95%
|
|
With
[Pd{C6H4(CH2N(CH2Ph)2)}(μ-Br)]2; tetrabutylammomium bromide; potassium carbonate;
In
N,N-dimethyl-formamide;
at 130 ℃;
for 0.166667h;
Microwave irradiation;
|
68%
|
|
With
C20H28Br2N2O4Pd2; potassium carbonate;
In
N,N-dimethyl-formamide;
at 130 ℃;
for 0.333333h;
Inert atmosphere;
Microwave irradiation;
|
57%
|
6136-68-1 Upstream products
-
99-03-6
1-(3-aminophenyl)ethanone
-
79784-56-8
m-cyanovalerophenone
-
107496-42-4
3-(1-Methoxyimino-ethyl)-benzonitrile
-
186581-53-3
diazomethane
6136-68-1 Downstream products
-
107100-94-7
(E)-3-(4-oxo-4-phenylbut-2-enoyl)benzonitrile
-
586-42-5
3-acetylbenzoic acid
-
105802-54-8
3-(2-oxoacetyl)benzonitrile
-
76597-77-8
3-cyanophenacyl chloride