4-Octyloxybenzaldehyde

Base Information

• Chemical Name: 4-Octyloxybenzaldehyde
• CAS No.: 24083-13-4
• Molecular Formula: C15H22O2
• Molecular Weight: 234.338
• Hs Code.: 29130000
• European Community (EC) Number: 246-012-1
• UNII: XQW85F9K7B
• DSSTox Substance ID: DTXSID5066954
• Nikkaji Number: J30.710F
• Wikidata: Q81993534
• Mol file: 24083-13-4.mol

Synonyms:4-(octyloxy)benzaldehyde;24083-13-4;4-Octyloxybenzaldehyde;4-n-Octyloxybenzaldehyde;4-octoxybenzaldehyde;Benzaldehyde, 4-(octyloxy)-;p-Octyloxybenzaldehyde;p-(Octyloxy)benzaldehyde;XQW85F9K7B;EINECS 246-012-1;4-octyloxy benzaldehyde;p-n-Octoxy benzaldehyde;p-n-Octyloxybenzaldehyde;UNII-XQW85F9K7B;SCHEMBL78962;LCZC1720;DTXSID5066954;4-n-Octyloxybenzaldehyde, >/=98%;MFCD00014136;STK503615;AKOS001053238;AS-58230;CS-0198792;FT-0638386;O0116;EN300-17353;D91802;Z56922117

Chemical Property of 4-Octyloxybenzaldehyde

Chemical Property:

• Appearance/Colour: clear colouless to yellowish liquid
• Vapor Pressure: 4.55E-05mmHg at 25°C
• Refractive Index: 1.52-1.522
• Boiling Point: 349.9 °C at 760 mmHg
• Flash Point: 142.9 °C
• PSA: 26.30000
• Density: 0.973 g/cm³
• LogP: 4.23840
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Sensitive.: Air Sensitive
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 9
• Exact Mass: 234.161979940
• Heavy Atom Count: 17
• Complexity: 183

Purity/Quality:

97% ^*data from raw suppliers

4-(Octyloxy)benzaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Benzaldehydes
• Canonical SMILES: CCCCCCCCOC1=CC=C(C=C1)C=O

Technology Process of 4-Octyloxybenzaldehyde

There total 18 articles about 4-Octyloxybenzaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

1-bromo-octane (111-83-1) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 4-octyloxybenzaldehyde (24083-13-4)

Guidance literature:

With potassium hydroxide; In acetonitrile; Heating;

DOI:10.5935/0103-5053.20150011

Reference yield: 94.0%

1-Iodooctane (629-27-6) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 4-octyloxybenzaldehyde (24083-13-4)

Guidance literature:

With potassium carbonate; In butanone; for 24h; Heating;

DOI:10.1016/j.bmc.2003.08.012

Reference yield: 88.0%

p-n-octyloxybenzyl alcohol (67698-68-4) → 4-octyloxybenzaldehyde (24083-13-4)

Guidance literature:

With manganese(IV) oxide; In chloroform; at 21 ℃; for 72h; Sealed tube;

DOI:10.1039/c5ob00621j

upstream raw materials:

1-Iodooctane

4-hydroxy-benzaldehyde

1-bromo-octane

1-bromo-4-octyloxybenzene

Downstream raw materials:

4,4'-di-n-octyloxybenzalazine

N-(4-octyloxy-benzylidene)-p-phenetidine

4-(4-Octyloxy-benzylamino)-benzoic acid

2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-5,15-bis(pyridin-4-yl)porphyrin