CAS 4903-09-7
:3-Chloro-4-methoxybenzaldehyde
Description:
3-Chloro-4-methoxybenzaldehyde, with the CAS number 4903-09-7, is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group. It consists of a benzene ring substituted with a chlorine atom at the meta position (3-position) and a methoxy group (-OCH3) at the para position (4-position). This compound typically appears as a pale yellow to light brown liquid or solid, depending on its purity and form. It is known for its distinctive aromatic odor and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. The presence of the chlorine and methoxy substituents influences its reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. Additionally, it may exhibit biological activity, which can be explored in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C8H7ClO2
InChI:InChI=1S/C8H7ClO2/c1-11-8-3-2-6(5-10)4-7(8)9/h2-5H,1H3
InChI key:InChIKey=WYVGYYIZXPXHAZ-UHFFFAOYSA-N
SMILES:C(=O)C1=CC(Cl)=C(OC)C=C1
Synonyms:- 3-Chloro-p-anisaldehyde
- 3-Chloroanisaldehyde
- 4-Methoxy-3-chlorobenzaldehyde
- Benzaldehyde, 3-chloro-4-methoxy-
- p-Anisaldehyde, 3-chloro-
- 3-Chloro-4-methoxybenzaldehyde
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Found 5 products.
3-Chloro-p-anisaldehyde
CAS:Formula:C8H7ClO2Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:170.593-Chloro-4-methoxybenzaldehyde
CAS:Formula:C8H7ClO2Purity:95%Color and Shape:SolidMolecular weight:170.59303-Chloro-4-methoxybenzaldehyde
CAS:<p>3-Chloro-4-methoxybenzaldehyde</p>Formula:C8H7ClO2Purity:98%Color and Shape: faint yellow crystalline powderMolecular weight:170.59g/mol3-Chloro-4-methoxybenzaldehyde
CAS:<p>3-Chloro-4-methoxybenzaldehyde is a chemical compound that belongs to the class of aromatic compounds. It is synthesized by reacting 3-chlorobenzaldehyde with methoxyacetone in a hydroxylation reaction. The asymmetric synthesis of 3-chloro-4-methoxybenzaldehyde was achieved by using a chiral auxiliary, which is an organic molecule that can be used to control the stereochemistry of other reactions. This product has high cytotoxicity and is able to cause melanogenesis (production of melanin) when applied to rat striatal membranes.</p>Formula:C8H7ClO2Purity:Min. 95%Color and Shape:PowderMolecular weight:170.59 g/mol3-Chloro-4-methoxybenzaldehyde
CAS:Formula:C8H7ClO2Purity:95%Color and Shape:Solid, Light grey powderMolecular weight:170.59




