24083-17-8

Basic information

• Product Name: 2-(dodecyloxy)benzaldehyde
• CAS NO: 24083-17-8
• Molecular Formula: C₁₉H₃₀O₂
• Molecular Weight: 290.4403
• Mol File: 24083-17-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 403.4°C at 760 mmHg
• Flash Point: 154.2°C
• Density: 0.947g/cm³
• Vapor Pressure: 1.02E-06mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: 2-(dodecyloxy)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dodecyloxy)benzaldehyde(24083-17-8)
• EPA Substance Registry System: 2-(dodecyloxy)benzaldehyde(24083-17-8)

Safety Data

• Hazardous Substances Data: 24083-17-8(Hazardous Substances Data)

Usage

Chemical structure

A benzene ring with a dodecyl group attached to the oxygen atom and an aldehyde functional group attached to the carbon atom.

Usage

Often used in the production of fragrances and flavors due to its aromatic properties.

Industry applications

Potential applications in the cosmetics and personal care industries as a fragrance ingredient.

Manufacturing

May be used in the manufacturing of chemical intermediates and as a solvent in various industrial processes.

Safety precautions

Should be handled and used with proper caution as it may have potential hazards and health risks.

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 143-15-7 1-dodecylbromide 
• 90-02-8 salicylaldehyde 
• 4292-19-7 1-Iodododecane 
• 10157-76-3 dodecyl 4-methylbenzenesulphonate 

Downstream Products

• 1176728-00-9 2-dodecyloxy-5-nitrobenzaldehyde 
• 112562-39-7 2-(2-Dodecyloxy-phenyl)-thiazolidine-3-carbothioic acid methylamide 

Relevant articles and documents

Acid-alkaline degradation of the anionic surface active agent and its application

The present invention discloses a structural formula (I) Compound and its use in the polymerization of the emulsion. And discloses the preparation process, using the compound prepared by the acid-base under the conditions of the rapid decomposition of the

Natural α-methylenelactam analogues: Design, synthesis and evaluation of α-alkenyl-γ and δ-lactams as potential antifungal agents against Colletotrichum orbiculare

In our continued efforts to improve the potential utility of the α-methylene-γ-lactone scaffold, 62 new and 59 known natural α-methylenelactam analogues including α-methylene-γ-lactams, α-arylidene-γ and δ-lactams, and 3-arylideneindolin-2-ones were synthesized as the bioisosteric analogues of the α-methylenelactone scaffold. The results of antifungal and cytotoxic activity indicated that among these derivatives compound (E)-1-(2, 6-dichlorobenzyl)-3-(2-fluorobenzylidene) pyrrolidin-2-one (Py51) possessed good selectivity with the highest antifungal activity against Colletotrichum orbiculare with IC50?=?10.4?μM but less cytotoxic activity with IC50?=?141.2?μM (against HepG2 cell line) and 161.2?μM (against human hepatic L02?cell line). Ultrastructural change studies performed by transmission electron microscope showed that Py51 could cause important cell morphological changes in C.?orbiculare, such as plasma membrane detached from cell wall, cell wall thickening, mitochondria disruption, a dramatic increase in vacuolation, and eventually a complete loss in the integrity of organelles. Significantly, mitochondria appeared one of the primary targets, as confirmed by their remarkably aberrant morphological changes. Analysis of structure–activity relationships revealed that incorporation of the aryl group into the α-exo-methylene and the N-benzyl substitution increased the activity. Meanwhile, the α-arylidene-γ-lactams have superiority in selectivity over the 3-arylideneindolin-2-ones. Based on the results, the N-benzyl substituted α-(2-fluorophenyl)-γ-lactam was identified as the most promising natural-based scaffold for further discovering and developing improved crop-protection agents.

Benzophenanthrene dodecyloxy bridged dodecyloxy phenyl porphyrin binary compound discotic liquid crystal material synthesis method

The invention discloses a benzophenanthrene dodecyloxy bridged dodecyloxy phenyl porphyrin binary compound discotic liquid crystal material synthesis method. The method includes: step one, generating monohydroxy pentahexyloxy benzophenanthrene, and synthe