p-Nonyloxybenzaldehyde

Base Information

• Chemical Name: p-Nonyloxybenzaldehyde
• CAS No.: 50262-46-9
• Molecular Formula: C16H24 O2
• Molecular Weight: 248.365
• Hs Code.: 2912499000
• DSSTox Substance ID: DTXSID20198256
• Nikkaji Number: J2.685.677I
• Wikidata: Q83071030
• Mol file: 50262-46-9.mol

Synonyms:p-Nonyloxybenzaldehyde;50262-46-9;4-n-Nonyloxybenzaldehyde;4-Nonyloxybenzaldehyde;4-nonoxybenzaldehyde;4-(Nonyloxy)benzaldehyde;(4-(nonyloxy)benzaldehyde);4-(Nonyloxy)benzaldehyde #;SCHEMBL1164477;DTXSID20198256;MFCD00043712;AKOS008968116;AS-77293;CS-0453114;FT-0639891;A828034

Chemical Property of p-Nonyloxybenzaldehyde

Chemical Property:

• Vapor Pressure: 1.64E-05mmHg at 25°C
• Melting Point: 140 °C
• Refractive Index: 1.5190
• Boiling Point: 180-182°C 4mm
• Flash Point: 180-182°C/4mm
• PSA: 26.30000
• Density: 0.965g/cm³
• LogP: 4.62850
• Sensitive.: Air Sensitive
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 248.177630004
• Heavy Atom Count: 18
• Complexity: 195

Purity/Quality:

99% ^*data from raw suppliers

4-N-Nonyloxybenzaldehyde ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

Useful:

• Canonical SMILES: CCCCCCCCCOC1=CC=C(C=C1)C=O

Technology Process of p-Nonyloxybenzaldehyde

There total 6 articles about p-Nonyloxybenzaldehyde 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: 90.0%

1-Bromononane (693-58-3) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 4-nonyloxy-benzaldehyde (50262-46-9)

Guidance literature:

With potassium carbonate; In acetonitrile; Reflux;

DOI:10.1016/j.tetlet.2010.09.077

Reference yield: 79.0%

→ 4-nonyloxy-benzaldehyde (50262-46-9)

Guidance literature:

Reference yield:

1-Chlorononane (2473-01-0) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 4-nonyloxy-benzaldehyde (50262-46-9)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃;

DOI:10.1016/j.bioorg.2020.104170

upstream raw materials:

1-iodononane

4-hydroxy-benzaldehyde

1-Bromononane

1-Chlorononane

Downstream raw materials:

C₃₁H₄₃NO₃

C₁₇H₂₇N₃OS

9O-PBT-12

9O-PBT

Refernces

• 1、 Velappan, Anand Babu,Kesamsetty, Dhanunjaya,Datta, Dhrubajyoti,Ma, Rui,Hari, Natarajan,Franzblau, Scott G.,Debnath, Joy. "1,3-Oxazine-2-one derived dual-targeted molecules against replicating and non-replicating forms of Mycobacterium tuberculosis". supporting information. . Retrieved 2020/10/02.
• 2、 Awad, Adil A.,Omarali, Al-Ameen Bariz,Al-Karawi, Ahmed Jasim M.,Al-Qaisi, Zyad Hussein J.,Majeed, Samer Ghanim. "Mesomorphism behaviour and photoluminescent properties of new asymmetrical 1,2-di(4-alkoxybenzylidene) hydrazines". . p. 67 - 77. Retrieved 2019/06/21.