CAS 61563-28-8

2-Chloro-3-methylbenzaldehyde

Description:

2-Chloro-3-methylbenzaldehyde, with the CAS number 61563-28-8, is an aromatic aldehyde characterized by the presence of both a chloro group and a methyl group on a benzene ring, specifically at the 2 and 3 positions, respectively. This compound typically appears as a colorless to pale yellow liquid with a distinct aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. The presence of the aldehyde functional group (-CHO) makes it reactive, particularly in nucleophilic addition reactions. Additionally, the chloro substituent can influence its reactivity and stability, making it a useful intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Safety precautions should be observed when handling this compound, as it may pose health risks through inhalation or skin contact. Overall, 2-Chloro-3-methylbenzaldehyde is a valuable compound in synthetic organic chemistry.

Formula: C₈H₇ClO

InChI: InChI=1/C8H7ClO/c1-6-3-2-4-7(5-10)8(6)9/h2-5H,1H3

SMILES: Cc1cccc(C=O)c1Cl

Synonyms:

• Benzaldehyde, 2-chloro-3-methyl-
• 2-Chloro-3-methylbenzaldehyde 95+%
• 2-CHLORO-3-METHYLBENZAL DEHYDE

2-CHLORO-3-METHYLBENZAL DEHYDE

CAS: 61563-28-8

Formula: C₈H₇ClO

Purity: 95%

Color and Shape: Solid

Molecular weight: 154.5936

Ref: IN-DA00EE56

2-Chloro-3-methylbenzaldehyde

CAS: 61563-28-8

2-Chloro-3-methylbenzaldehyde

Purity: 95%

Color and Shape: Solid

Molecular weight: 154.59g/mol

Ref: 54-OR54473

2-Chloro-3-methylbenzaldehyde

CAS: 61563-28-8

Formula: C₈H₇ClO

Purity: 98%

Color and Shape: Solid, Low Melting Solid

Molecular weight: 154.59

Ref: 10-F037515

2-Chloro-3-methylbenzaldehyde

CAS: 61563-28-8

2-Chloro-3-methylbenzaldehyde is a reagent that is used in organic synthesis. It is an isomeric form of 2-chlorobenzaldehyde. 2-Chloro-3-methylbenzaldehyde can be prepared by the reaction of benzaldehyde with magnesium, which produces chloral and methyl alcohol. The chloride ion then reacts with the methyl alcohol to produce 2-chloro-3-methylbenzaldehyde. It has been shown that it can be used as a grignard reagent to make substituted ketones or esters. This compound also exhibits dihedral symmetry and has two planar forms, one of which is more stable than the other in solution.

Formula: C₈H₇ClO

Purity: Min. 95%

Molecular weight: 154.6 g/mol

Ref: 3D-LCA56328