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Methyl 2-chlorobenzoate

  • CasNo:610-96-8

Product Description

Quality manufacturer supply Methyl 2-chlorobenzoate 610-96-8 in stock with high standard

  • Molecular Formula: C8H7ClO2
  • Molecular Weight: 170.595
  • Appearance/Colour: White to light yellow crystal powder 
  • Vapor Pressure: 0.0868mmHg at 25°C 
  • Melting Point: 233-235 °C 
  • Refractive Index: 1.5351-1.537  
  • Boiling Point: 225.4 °C at 760 mmHg 
  • Flash Point: 101.7 °C 
  • PSA: 26.30000 
  • Density: 1.224 g/cm3 
  • LogP: 2.12660 

Methyl 2-chlorobenzoate(Cas 610-96-8) Usage

General Description

Methyl 2-chlorobenzoate, a methyl 2-halobenzoate, is an ester. It can be synthesized from 2-chlorobenzoyl chloride. Its reduction with NaBH4 in diglyme at 162°C affords 2-chlorobenzyl alcohol.

InChI:InChI=1/C8H7ClO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,1H3

610-96-8 Relevant articles

Oxidative Coupling of Aldehydes with Alcohol for the Synthesis of Esters Promoted by Polystyrene-Supported N-Heterocyclic Carbene: Unraveling the Solvent Effect on the Catalyst Behavior Using NMR Relaxation

Di Carmine, Graziano,Ragno, Daniele,Massi, Alessandro,D'agostino, Carmine

, p. 4927 - 4931 (2020)

Heterogeneous organocatalysts hold great...

A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen

Anwar, Muhammad,Beller, Matthias,Dastgir, Sarim,Junge, Kathrin,Leonard, David K.,Ryabchuk, Pavel

, (2022/02/03)

Hydrodehalogenation is an effective stra...

Br?nsted acid-catalyzed chlorination of aromatic carboxylic acids

Yu, Zhiqun,Yao, Hongmiao,Xu, Qilin,Liu, Jiming,Le, Xingmao,Ren, Minna

supporting information, p. 685 - 689 (2021/04/09)

The chlorination of aromatic carboxylic ...

Preparation method of methyl benzoate compound

-

Paragraph 0019; 0037-0038, (2021/08/14)

A preparation method of a methyl benzoat...

Antibacterial and Antiviral Activities of 1,3,4-Oxadiazole Thioether 4H-Chromen-4-one Derivatives

Cao, Xiao,Liu, Fang,Liu, Liwei,Liu, Tingting,Peng, Feng,Wang, Qifan,Xie, Chengwei,Xue, Wei,Yang, Jinsong

, p. 11085 - 11094 (2021/10/01)

Various 1,3,4-oxadiazole thioether 4H-ch...

610-96-8 Process route

methanol
67-56-1

methanol

o-chlorobenzoyl chloride
609-65-4

o-chlorobenzoyl chloride

methyl chlorobenzoate
610-96-8

methyl chlorobenzoate

Conditions
Conditions Yield
With triethylamine; at 20 ℃; for 10h;
95%
With triethylamine; In dichloromethane; at 0 ℃;
With triethylamine; In dichloromethane; at 0 ℃; Inert atmosphere;
1.57 g
methanol
67-56-1

methanol

ortho-chlorobenzoic acid
118-91-2

ortho-chlorobenzoic acid

methyl chlorobenzoate
610-96-8

methyl chlorobenzoate

Conditions
Conditions Yield
With sulfuric acid; for 4h; Reflux;
100%
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; at 60 ℃; for 8h;
100%
With sulfuric acid; Heating;
99%
With 1,3,5-trichloro-2,4,6-triazine; sodium carbonate; at 50 ℃; for 0.333333h; Sonication;
94%
With sulfuric acid; at 78 ℃; for 8h;
94.5%
With thionyl chloride; for 3h; Ambient temperature;
91%
Acidic conditions;
86%
sulfuric acid;
81%
With sulfuric acid; at 20 ℃; for 12h; Inert atmosphere;
80%
With Oxone; In toluene; at 60 ℃; for 48h; Green chemistry;
74%
With sulfuric acid; for 10h; Reflux;
60%
acid; at 30 ℃; Rate constant;
With hydrogenchloride;
With sulfuric acid;
With diethyl ether; boron trifluoride;
With sulfuric acid; at 100 ℃; for 0.0833333h; under 5171.62 Torr; Microwave irradiation;
With sulfuric acid; Reflux;
Acidic conditions; Reflux;
With sulfuric acid; for 4h; Reflux;
With sulfuric acid; Inert atmosphere; Reflux;
Reflux; Acidic conditions;
With sulfuric acid; Reflux;
With sulfuric acid; Reflux;
Acidic conditions; Reflux;
With sulfuric acid;
With sulfuric acid; for 4h; Reflux;
With sulfuric acid; for 6h; Reflux;
With sulfuric acid; Reflux;
With sulfuric acid; at 70 ℃; for 10h;
Acidic conditions;
With sulfuric acid; for 24h; Reflux;
With glycerol-based sulfonic acid functionalized carbon catalyst; for 6h; Reflux; Green chemistry;
With thionyl chloride; at 20 ℃;
With sulfuric acid; for 5h; Reflux;
methanol; ortho-chlorobenzoic acid; at 0 ℃; for 0.166667h;
With thionyl chloride; for 6h; Reflux;
With sulfuric acid; Reflux;
With sulfuric acid; Reflux;
With sulfuric acid; at 85 ℃;
With sulfuric acid; for 2h; Reflux;
With sulfuric acid;
With sulfuric acid; for 5h; Reflux;
With sulfuric acid; for 8h; Reflux;
With sulfuric acid; for 8h; Reflux;
With thionyl chloride; at 20 ℃; for 3h; Reflux;
With sulfuric acid; for 3h; Reflux;

610-96-8 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 609-65-4
    609-65-4

    o-chlorobenzoyl chloride

  • 118-91-2
    118-91-2

    ortho-chlorobenzoic acid

  • 57031-51-3
    57031-51-3

    Methyl-tert.-butylperoxyoxalat

610-96-8 Downstream products

  • 100398-32-1
    100398-32-1

    2-(2'-pyrido)-2-chloroacetophenone

  • 7579-40-0
    7579-40-0

    benzyl 2-chlorobenzoate

  • 3670-15-3
    3670-15-3

    2-(2-chlorophenyl)propan-2-ol

  • 97221-97-1
    97221-97-1

    2-chloro-benzoic acid dodecyl ester

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