CAS 117490-57-0
:Benzaldehyde, 2-chloro-4-(phenylmethoxy)-
Description:
Benzaldehyde, 2-chloro-4-(phenylmethoxy)-, also known by its CAS number 117490-57-0, is an organic compound characterized by its aromatic structure. It features a benzaldehyde moiety, which is a benzene ring with a formyl group (-CHO), and a chloro substituent at the second position of the ring. Additionally, it has a phenylmethoxy group, indicating the presence of a methoxy group (-O-CH2-Ph) attached to the fourth position of the benzene ring. This compound is typically a colorless to pale yellow liquid with a distinct aromatic odor. It is soluble in organic solvents and exhibits moderate polarity due to the presence of both the aldehyde and ether functionalities. The presence of chlorine in its structure may impart unique reactivity, making it useful in various synthetic applications, including as an intermediate in organic synthesis. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C14H11ClO2
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Found 3 products.
4-(Benzyloxy)-2-chlorobenzaldehyde
CAS:<p>4-(Benzyloxy)-2-chlorobenzaldehyde is an aldehyde that can be used for the synthesis of organic compounds. It is made from 2-chloro-4-hydroxybenzaldehyde, which is synthesized from hydroxybenzaldehyde, oxime, and benzyl alcohol. The product has been shown to react with riboflavin and a second reagent in the presence of palladium to form a chromatographic column. 4-(Benzyloxy)-2-chlorobenzaldehyde reacts with 6-chlorouracil to form an oxirane ring. This reaction can also be used to synthesize tulobuterol, which is a β2-agonist. 4-(Benzyloxy)-2-chlorobenzaldehyde reacts with ribose in the presence of hydroxy to produce glucose and 2-(6'-hydroxypurinomethyl)riboflavin as a byproduct.</p>Formula:C14H11ClO2Purity:Min. 95%Molecular weight:246.69 g/mol
