24083-06-5

Basic information

• Product Name: 3-PENTYLOXY-BENZALDEHYDE
• Synonyms: 3-PENTYLOXY-BENZALDEHYDE;3-amoxybenzaldehyde;3-pentoxybenzaldehyde;ZINC02387659
• CAS NO: 24083-06-5
• Molecular Formula: C₁₂H₁₆O₂
• Molecular Weight: 192.25
• Mol File: 24083-06-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-PENTYLOXY-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-PENTYLOXY-BENZALDEHYDE(24083-06-5)
• EPA Substance Registry System: 3-PENTYLOXY-BENZALDEHYDE(24083-06-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 24083-06-5(Hazardous Substances Data)

Upstream product

• 628-17-1 amyl iodide 
• 100-83-4 meta-hydroxybenzaldehyde 
• 71-41-0 pentan-1-ol 
• 110-53-2 1-Bromopentane 

Downstream Products

• 110698-30-1 m-pentyloxybenzoic acid 
• 32223-66-8 3-n-pentyloxyphenylisocyanate 
• 1362626-27-4 C₂₀H₂₆N₂O₂ 
• 1075741-32-0 3-[3-(n-pentyloxy)phenyl]-1,3-dihydro-1-isobenzofuranone 
• 321581-74-2 6-(3-pentyloxy-phenyl)-hexane-1,2,4-triol 
• 307498-66-4 3-hydroxy-5-(3-pentyloxy-phenyl)-pentanoic acid 
• 307498-63-1 1-(3-pentyloxy-phenyl)-hex-5-en-3-ol 
• 307498-56-2 3-(3-pentyloxy-phenyl)-propionaldehyde 
• 307498-55-1 (E)-3-(3-Pentyloxy-phenyl)-propenal 

Relevant articles and documents

ALKOXYBENZALDEHYDE DERIVATIVES AND PRECURSORS THEREOF

The present invention refers to alkoxybenzaldehyde derivatives and precursors thereof. The invention further refers to perfume compositions and fragranced article comprising them.

cis-Cinnamic acid selective suppressors distinct from auxin inhibitors

The activity of cis-cinnamic acid (cis-CA), one of the allelochemicals, in plants is very similar to that of indole-3-acetic acid (IAA), a natural auxin, and thus cis-CA has long been believed to be an analog of auxin. We have reported some structure-acti

Potential modes of interaction of 9-aminomethyl-9,10-dihydroanthracene (AMDA) derivatives with the 5-HT2A receptor: A ligand structure-affinity relationship, receptor mutagenesis and receptor modeling investigation

The effects of 3-position substitution of 9-aminomethy 1-9,10- dihydroanthracene (AMDA) on 5-HT2A receptor affinity were determined and compared to a parallel series of DOB-like 1-(2,5-dimethoxyphenyl)-2- aminopropanes substituted at the 4-position. The results were interpreted within the context of 5-HT2A receptor models that suggest that members of the DOB-like series can bind to the receptor in two distinct modes that correlate with the compounds' functional activity. Automated ligand docking and molecular dynamics suggest that all of the AMDA derivatives, the parent of which is a 5-HT2A antagonist, bind in a fashion analogous to that for the sterically demanding antagonist DOB-like compounds. The failure of the F340 6.52L mutation to adversely affect the affinity of AMDA and the 3-bromo derivative is consistent with the proposed modes of orientation. Evaluation of ligand-receptor complex models suggest that a valine/threonine exchange between the 5-HT2A and D2 receptors may be the origin of selectivity for AMDA and two substituted derivatives.