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| Chemical Description | 2-chlorobenzaldehyde is an organic compound with a chlorinated benzene ring and an aldehyde functional group. | 
| Preparation | 2-Chlorobenzaldehyde is produced mainly by chlorination of 2-chlorotoluene to form 2-chlorobenzal chloride, which is then subjected to acid hydrolysis. Metal salts, such as iron(III) chloride, are used as catalysts. The hydrolysis can also be accomplished using formic acid without a catalyst.2-Chlorobenzaldehyde can also be produced by oxidation of 2-chlorobenzyl chloride with N-oxides of tertiary amines or with dilute nitric acid.https://pubchem.ncbi.nlm.nih.gov/compound/2-Chlorobenzaldehyde | 
| Application | 2-Chlorobenzaldehyde is used acid zinc plating brightener, also be used for organic synthesis, agricultural pesticide and pharmaceutical industries. It is used to synthesize the acaricides clofentezine and flutenzine. 2-Chlorobenzaldehyde undergoes alkynylation with phenylacetylene in the presence of catalytic ligands and dimethylzinc at 0°C to form binaphthyl-derived amino alcohols. | 
| Synthesis Reference(s) | Tetrahedron Letters, 34, p. 8037, 1993 DOI: 10.1016/S0040-4039(00)61444-2 | 
| General Description | 2-chlorobenzaldehyde is a clear colorless to yellowish liquid. (NTP, 1992) | 
| Air & Water Reactions | 2-Chlorobenzaldehyde is moisture and light sensitive. Slightly water soluble. | 
| Reactivity Profile | 2-Chlorobenzaldehyde reacts with iron and strong oxidizers, strong bases and strong reducing agents. | 
| Health Hazard | Symptoms of exposure to 2-Chlorobenzaldehyde may include skin, eye and upper respiratory tract irritation. This compound may cause skin, eye and respiratory tract irritation. When heated to decomposition it emits toxic fumes. | 
| Fire Hazard | 2-Chlorobenzaldehyde is combustible. | 
| Safety Profile | Poison by intraperitoneal and intravenous routes. When heated to decomposition it emits toxic fumes of Cl-. See also ALDEHYDES and CHLORIDES. | 
| Purification Methods | Wash it with 10% Na2CO3 solution, then fractionally distil it in the presence of a small amount of catechol as stabiliser. [Beilstein 7 H 233, 7 IV 561.] | 
InChI:InChI=1/C7H5ClO/c8-7-4-2-1-3-6(7)5-9/h1-5H
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2-methylchlorobenzene


2-chloro-benzaldehyde


1-bromomethyl-2-chlorobenzene


ortho-chlorobenzoic acid
| 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% | 

o-chlorobenzoyl chloride


2-Chlorobenzyl alcohol


2-chloro-benzaldehyde
| Conditions | Yield | 
|---|---|
| With    pyridine; sodium tetrahydroborate;     In   tetrahydrofuran; N,N-dimethyl-formamide;   at 0 ℃; for 0.0166667h; Product distribution; other borane scavengers;  | 

quinoline

meta-dinitrobenzene

2-Chlorobenzyl alcohol

sodium carbonate

3-(2-chlorophenyl)-2-methylacrylic acid

1-[(2-chlorophenyl)(piperidin-1-yl)methyl]naphthalen-2-ol

α-(2-chlorophenyl)-4-morpholineacetonitrile

(2-chloro-phenyl)-dimorpholino-methane
