CAS 2426-87-1
:4-Benzyloxy-3-methoxybenzaldehyde
Description:
4-Benzyloxy-3-methoxybenzaldehyde, with the CAS number 2426-87-1, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. This compound features a methoxy group (-OCH3) and a benzyloxy group (-O-Ph) attached to a benzene ring, contributing to its overall reactivity and solubility properties. It typically appears as a pale yellow to light brown solid or liquid, depending on its purity and form. The presence of the aldehyde group makes it a potential candidate for various chemical reactions, including nucleophilic additions and condensation reactions. Its functional groups also suggest that it may exhibit interesting biological activities, making it of interest in medicinal chemistry and organic synthesis. Additionally, the compound's solubility in organic solvents like ethanol and dichloromethane facilitates its use in laboratory settings. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.
Formula:C15H14O3
InChI:InChI=1/C15H14O3/c1-17-14-8-7-13(10-16)9-15(14)18-11-12-5-3-2-4-6-12/h2-10H,11H2,1H3
InChI key:InChIKey=JSHLOPGSDZTEGQ-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(OC)C=C(C=O)C=C2
Synonyms:- 3-(Benzyloxy)-4-Methoxybenzaldehyde
- 3-Methoxy-4-(benzyloxy)benzaldehyde
- 3-Methoxy-4-(phenylmethoxy)benzaldehyde
- 4-(Benzyloxy)-3-Methoxy Benzaldehyde
- 4-O-Benzylvanillin
- Benzaldehyde, 3-methoxy-4-(phenylmethoxy)-
- Benzaldehyde, 4-(benzyloxy)-3-methoxy-
- Benzylvanillin
- NSC 208757
- NSC 22599
- NSC 44876
- Vanillin benzyl ether
- o-Benzylvanillin
- 4-(Benzyloxy)-3-methoxybenzaldehyde
- Benzaldehyde, 4-benzyloxy-5-methoxy-
- ZERENEX E/4048067
- O-BENZYLOXYVANILLIN
- 3-METHOXY-4-(N-PIPERIDINOMETHYL OXO)-BENZALDELYDE
- 4-BENZYLOXY-3-METHYLBENZALDEHYDE
- 4-BENZYLOXY-3-METHOXYBENZALDEHYDE 98%
- BENZYL VANILLIN
- AKOS BBS-00003156
- LABOTEST-BB LT00053610
- ASISCHEM N39068
- OTAVA-BB BB7018801951
- O-BENZYLOXYVANILLIN (4-BENZYLOXY-3-METHOXYBENZALDEHYDE)
- See more synonyms
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Found 8 products.
4-Benzyloxy-3-methoxybenzaldehyde
CAS:Formula:C15H14O3Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:242.274-Benzyloxy-3-methoxybenzaldehyde, 98%
CAS:<p>4-Benzyloxy-3-methoxybenzaldehyde was used in the synthesis of 1,2-bis(4-benzyloxy-3-methoxyphenyl)-3-hydroxy-propionic acid1. It was also used in first enantioselective total synthesis of a neurotrophic (-)-talaumidin. 4-Benzyloxy-3-methoxybenzaldehyde reacts with benzohydrazide to yield (E)-N?-(4-</p>Formula:C15H14O3Purity:98%Color and Shape:Crystals or powder or crystalline powder, White to pale yellowMolecular weight:242.274-Benzyloxy-3-methoxybenzaldehyde
CAS:Formula:C15H14O3Purity:95%Color and Shape:SolidMolecular weight:242.26994-(Benzyloxy)-3-methoxybenzaldehyde
CAS:<p>4-(Benzyloxy)-3-methoxybenzaldehyde</p>Formula:C15H14O3Purity:≥95%Color and Shape: white crystalline powderMolecular weight:242.27g/mol4-Benzyloxy-3-methoxybenzaldehyde
CAS:<p>4-Benzyloxy-3-methoxybenzaldehyde is a deuterium isotope analog of the natural compound benzaldehyde. This molecule has been shown to inhibit the growth of cancer cells in tissue culture by binding to DNA. The molecular mechanism of this inhibition is believed to involve an enzymatic process that results in the substitution of chloride for chlorine, thereby inhibiting DNA synthesis and preventing cell division. 4-Benzyloxy-3-methoxybenzaldehyde also inhibits the production of growth factors and thus has anticancer activity.</p>Formula:C15H14O3Purity:Min. 95%Color and Shape:PowderMolecular weight:242.27 g/mol4-Benzyloxy-3-methoxybenzaldehyde
CAS:Formula:C15H14O3Purity:95%Color and Shape:SolidMolecular weight:242.2744-Benzyloxy-3-methoxybenzaldehyde
CAS:Controlled ProductFormula:C15H14O3Color and Shape:NeatMolecular weight:242.27







