118-91-2

  • Product Name2-Chlorobenzoic acid
  • Molecular FormulaC7H5ClO2
  • Molecular Weight156.569
  • Purity99%
  • Appearancewhite crystals or powder
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Product Details

Quick Details

  • CasNo: 118-91-2
  • Molecular Formula: C7H5ClO2
  • Appearance: white crystals or powder
  • Purity: 99%

High Quality Chinese Factory supply 118-91-2 2-Chlorobenzoic acid

  • Molecular Formula:C7H5ClO2
  • Molecular Weight:156.569
  • Appearance/Colour:white crystals or powder 
  • Vapor Pressure:0.00242mmHg at 25°C 
  • Melting Point:139-143 °C 
  • Boiling Point:275.7 °C at 760 mmHg 
  • Flash Point:120.5 °C 
  • PSA:37.30000 
  • Density:1.544 g/cm3 
  • LogP:2.03820 

o-Chlorobenzoic acid(Cas 118-91-2) Usage

General Description

o-Chlorobenzoic acid is a simple organic compound with the chemical formula C7H5ClO2. It consists of a benzene ring bearing a carboxylic acid group and a chlorine atom at the ortho position. o-Chlorobenzoic acid is a white crystalline solid that is used in the synthesis of various pharmaceuticals, dyes, and agrochemicals. It is also used as an intermediate in the production of other chemicals. o-Chlorobenzoic acid is moderately toxic and may cause irritation to the skin, eyes, and respiratory system upon exposure. Additionally, it is not readily biodegradable and it poses a risk to the environment if released into water or soil.

InChI:InChI=1/C7H5ClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)/p-1

118-91-2 Relevant articles

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Atkinson et al.

, p. 476 (1943)

-

TiO2-mediated photomineralization of 2-chlorobiphenyl: The role of O2

Wang, Yongbing,Hong, Chia-Swee

, p. 2791 - 2797 (2000)

Photocatalytic mineralization of 2-chlor...

Oxidation of aromatic aldehydes with potassium bromate-bromide reagent and an acidic catalyst

Sharma,Robert, Alice R.

, p. 3251 - 3254 (2013)

We report herein an easy oxidation proce...

Bismuth(III)-catalyzed oxidative cleavage of aryl epoxides: substituent effects on the kinetics of the oxidation reaction

Boisselier, Veronique Le,Dunach, Elisabet,Postel, Michele

, p. 119 - 124 (1994)

Bismuth(III)mandelate catalyzes the oxid...

Chemiluminescence from arylcarbene oxidation: phenylchlorocarbene and (2-chlorophenyl)carbene

Sander, Wolfram W.

, p. 637 - 646 (1987)

Chemiluminescence is observed in the the...

Supported ruthenium hydride catalysts for direct conversion of alcohols to carboxylic acids using styrene oxide as oxidant

Ghafouri, Moloud,Moghadam, Majid,Mehrani, Kheirollah,Daneshvar, Anahita

, (2018)

In the present work, the ability of two ...

SELECTIVE REMOVAL OF ORTHO HALOGENS BY A DIORGANOLANTHANOID

Deacon, G.B.,MacKinnon, P.I.

, p. 783 - 784 (1984)

Reaction of halogenobenzoic acids with b...

COBALT CARBONYL-CATALYZED DOUBLE-CARBONYLATION OF O-HALOGENATED BENZOIC ACIDS UNDER PHOTOSTIMULATION

Kashimura, Tsugunori,,Kudo, Kiyoshi,Mori, Sadayuki,Sugita, Nobuyuki

, p. 483 - 486 (1986)

Cobalt carbonyl-catalyzed double-carbony...

Reductions and radical cyclizations of aryl and alkyl bromides mediated by NaBH4 in aqueous base

Rai, Roopa,Collum, David B.

, p. 6221 - 6224 (1994)

Reductions and free radical cyclizations...

Direct oxidation of alcohols to carboxylic acids over ruthenium hydride catalyst with diphenyl sulfoxide oxidant

Barati, Behjat,Moghadam, Majid,Rahmati, Abbas,Mirkhani, Valiollah,Tangestaninejad, Shahram,Mohammadpoor-Baltork, Iraj

, p. 114 - 117 (2013)

In the present work, a new method for th...

-

Atkinson et al.

, (1943)

-

Bimetallic oxide nanoparticles confined in ZIF-67-derived carbon for highly selective oxidation of saturated C–H bond in alkyl arenes

Huang, Cheng,Su, Xiaoyan,Gu, Xiangyu,Liu, Rui,Zhu, Hongjun

, (2020/10/15)

Zeolite imidazolate frameworks (ZIFs) ha...

Aerobic oxidation of aldehydes to carboxylic acids catalyzed by recyclable ag/c3 n4 catalyst

Wu, Chaolong,Yao, Xiaoquan,Yu, Min,Zhou, Li,Zhu, Li

, p. 167 - 175 (2021/03/19)

The oxidation of aldehydes is an efficie...

MOF-Zn-NHC as an efficient N-heterocyclic carbene catalyst for aerobic oxidation of aldehydes to their corresponding carboxylic acids: Via a cooperative geminal anomeric based oxidation

Babaee, Saeed,Zarei, Mahmoud,Zolfigol, Mohammad Ali

, p. 36230 - 36236 (2021/12/02)

As an efficient heterogenous N-heterocyc...

Cleavage of Carboxylic Esters by Aluminum and Iodine

Sang, Dayong,Yue, Huaxin,Fu, Yang,Tian, Juan

, p. 4254 - 4261 (2021/03/09)

A one-pot procedure for deprotecting car...

118-91-2 Process route

methanol
67-56-1

methanol

tetrachloromethane
56-23-5

tetrachloromethane

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

2-Chlorobenzyl alcohol
17849-38-6

2-Chlorobenzyl alcohol

ortho-chlorobenzoic acid
118-91-2

ortho-chlorobenzoic acid

Conditions
Conditions Yield
Kinetics; Disproportionierung;
 
2-methylchlorobenzene
95-49-8

2-methylchlorobenzene

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

1-bromomethyl-2-chlorobenzene
611-17-6

1-bromomethyl-2-chlorobenzene

ortho-chlorobenzoic acid
118-91-2

ortho-chlorobenzoic acid

Conditions
Conditions Yield
With oxygen; cobalt(II) acetate; sodium bromide; In acetic acid; at 95 ℃; for 0.666667h; Kinetics; Mechanism; Rate constant; other time; other temperature; various concentrations of Co(OAc)2 and NaBr;
96%
With oxygen; cobalt(II) acetate; sodium bromide; In acetic acid; at 95 ℃; for 0.666667h;
95%

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118-91-2 Downstream products

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  • 857601-70-8
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    N-(6-benzyloxy-[3]pyridyl)-anthranilic acid

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