20099-89-2

  • 产品名称:2-溴-4'-氰基苯乙酮
  • 分子式:C9H6BrNO
  • 纯度:99%
  • 分子量:224.057
询价

产品详情

pd_meltingpoint:92-96 °C(lit.)

外观:off-white to light yellow crystalline powder

 

  • Molecular Formula:C9H6BrNO
  • Molecular Weight:224.057
  • Appearance/Colour:off-white to light yellow crystalline powder 
  • Melting Point:92-96 °C(lit.) 
  • Refractive Index:1.59 
  • Boiling Point:342.4 °C at 760 mmHg 
  • Flash Point:160.9 °C 
  • PSA:40.86000 
  • Density:1.56 g/cm3 
  • LogP:2.13588 

4-CYANOPHENACYL BROMIDE(Cas 20099-89-2) Usage

Chemical Properties

off-white to light yellow crystalline powder

Uses

4-(2-Bromoacetyl)benzonitrile is useful for the irreversible inhibitory activity of Glycogen synthase kinase 3 (GSK-3). Phenylhalomethylketones can be used in the study of novel GSK-3 inhibitors.

General Description

2-Bromo-4′-cyanoacetophenone can be synthesized from ethylbenzene via aerobic photooxidation using aqueous HBr.

InChI:InChI=1/C10H7BrO/c1-2-8-3-5-9(6-4-8)10(12)7-11/h1,3-6H,7H2

20099-89-2 Relevant articles

Unexpected ritter reaction during acid-promoted 1,3-dithiol-2-one formation

Dumur, Frederic,Mayer, Cedric R.

, p. 889 - 896 (2013)

A series of aryl-substituted 1,3-dithiol...

Electroselective α-bromination of acetophenone using: In situ bromonium ions from ammonium bromide

Jagatheesan,Joseph Santhana Raj,Lawrence,Christopher

, p. 35602 - 35608 (2016)

A greener and expeditious method for the...

High Chemo-/Stereoselectivity for Synthesis of Polysubstituted Monofluorinated Pyrimidyl Enol Ether Derivatives

Kang, Lei,Wang, Fang,Zhang, Jinlong,Yang, Huameng,Xia, Chungu,Qian, Jinlong,Jiang, Gaoxi

supporting information, p. 1669 - 1674 (2021/03/08)

A novel intramolecular Smiles rearrangem...

Base-Catalyzed Intramolecular Defluorination/O-Arylation Reaction for the Synthesis of 3-Fluoro-1,4-oxathiine 4,4-Dioxide

Kang, Lei,Zhang, Jinlong,Yang, Huameng,Qian, Jinlong,Jiang, Gaoxi

supporting information, p. 785 - 789 (2021/04/09)

A novel process involving base-catalyzed...

An umpolung oxa-[2,3] sigmatropic rearrangement employing arynes for the synthesis of functionalized enol ethers

Gaykar, Rahul N.,George, Malini,Guin, Avishek,Bhattacharjee, Subrata,Biju, Akkattu T.

supporting information, p. 3447 - 3452 (2021/05/04)

An oxa-[2,3] sigmatropic rearrangement i...

Flexible on-site halogenation paired with hydrogenation using halide electrolysis

Shang, Xiao,Liu, Xuan,Sun, Yujie

supporting information, p. 2037 - 2043 (2021/03/26)

Direct electrochemical halogenation has ...

20099-89-2 Process route

methanol
67-56-1

methanol

4-(2,2,2-tribromoacetyl)benzonitrile

4-(2,2,2-tribromoacetyl)benzonitrile

4-cyanobenzoic acid methyl ester
1129-35-7

4-cyanobenzoic acid methyl ester

4-Cyanophenacyl bromide
20099-89-2

4-Cyanophenacyl bromide

methyl (4-cyanophenyl)glyoxylate
52798-47-7

methyl (4-cyanophenyl)glyoxylate

2,2-dibromo-1-(4-cyanophenyl)ethan-1-one
21661-87-0

2,2-dibromo-1-(4-cyanophenyl)ethan-1-one

Conditions
Conditions Yield
With oxygen; at 10 ℃; for 2h; Irradiation;
3.5 % Chromat.
5.4 % Chromat.
1 % Chromat.
59.0 % Chromat.
4-ethylbenzonitrile
25309-65-3

4-ethylbenzonitrile

4-cyanophenyl methyl ketone
1443-80-7

4-cyanophenyl methyl ketone

4-Cyanophenacyl bromide
20099-89-2

4-Cyanophenacyl bromide

Conditions
Conditions Yield
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); water; In acetonitrile; at 80 ℃; for 8h;
 

20099-89-2 Upstream products

  • 1443-80-7
    1443-80-7

    4-cyanophenyl methyl ketone

  • 67-56-1
    67-56-1

    methanol

  • 25309-65-3
    25309-65-3

    4-ethylbenzonitrile

  • 157729-39-0
    157729-39-0

    4-(2-bromoethynyl)-benzonitrile

20099-89-2 Downstream products

  • 100537-59-5
    100537-59-5

    4-[(pyridine-3-sulfonyl)-acetyl]-benzonitrile

  • 103962-24-9
    103962-24-9

    4-(2-[1,2,4]triazol-1-ylacetyl)benzonitrile

  • 94020-34-5
    94020-34-5

    ethyl 2-acetyl-4-(4-cyanophenyl)-4-oxobutanoate

  • 138470-03-8
    138470-03-8

    6-<5-<2-(4-Cyanphenacyloxy)-phenyl>-1,2,4-dithiazol-3-yliden>-2,4-cyclohexadien-1-on