1-Phenylnonan-1-one

Base Information

• Chemical Name: 1-Phenylnonan-1-one
• CAS No.: 6008-36-2
• Molecular Formula: C15H22 O
• Molecular Weight: 218.339
• Hs Code.: 2914399090
• European Community (EC) Number: 227-861-7
• UNII: DJ4KL5XS87
• DSSTox Substance ID: DTXSID70208819
• Nikkaji Number: J223.947G
• Wikidata: Q83082978
• Mol file: 6008-36-2.mol

Synonyms:1-Phenylnonan-1-one;n-Nonanophenone;6008-36-2;Nonanophenone;1-Phenyl-1-nonanone;n-Octyl phenyl ketone;1-Nonanone, 1-phenyl-;octyl phenyl ketone;DJ4KL5XS87;EINECS 227-861-7;Octylphenylketon;octylphenyl ketone;MFCD00048965;NONANOYLBENZENE;PELARGONOPHENONE;PELARGONYLBENZENE;1-phenyl-nonan-1-one;UNII-DJ4KL5XS87;SCHEMBL962848;DTXSID70208819;CHEBI:145973;AKOS009156600;AS-57233;CS-0206447;N0568;D91731;A869051

Chemical Property of 1-Phenylnonan-1-one

Chemical Property:

• Appearance/Colour: CLEAR COLOURLESS TO LIGHT YELLOW LIQUID
• Vapor Pressure: 0.000563mmHg at 25°C
• Melting Point: 14°C
• Refractive Index: 1.5005-1.5025
• Boiling Point: 139-140°C 2mm
• Flash Point: 139-140°C/2mm
• PSA: 17.07000
• Density: 0,94 g/cm3
• LogP: 4.61990
• XLogP3: 5.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 218.167065321
• Heavy Atom Count: 16
• Complexity: 180

Purity/Quality:

97% ^*data from raw suppliers

1-Phenyl-1-nonanone ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC(=O)C1=CC=CC=C1
• Uses: N-NONANOPHENONE is used in the synthesis of novel alkylbenzene sulfonate gemini surfactants. 1-Phenyl-1-nonanone is used in the synthesis of novel alkylbenzene sulfonate gemini surfactants.

Technology Process of 1-Phenylnonan-1-one

There total 93 articles about 1-Phenylnonan-1-one 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-phenylnonan-1-ol (57716-72-0,92660-98-5,131320-85-9,131320-86-0) → 1-phenylnonan-1-one (6008-36-2)

Guidance literature:

With iodine; potassium carbonate; In tert-butyl alcohol; at 90 ℃; for 6h;

DOI:10.1016/j.tet.2005.03.097

Reference yield: 99.0%

oct-1-ene (111-66-0,25068-25-1) + benzaldehyde (100-52-7) → 1-phenylnonan-1-one (6008-36-2)

Guidance literature:

With 3-methylpyridin-2-ylamine; aniline; benzoic acid; Wilkinson's catalyst; In toluene; at 130 ℃; for 1h;

DOI:10.1002/1521-3773(20000901)39:17<3070::AID-ANIE3070>3.0.CO;2-G

Reference yield: 99.0%

sodium nonanoate (14047-60-0) + phenylzinc iodide (23665-09-0) → 1-phenylnonan-1-one (6008-36-2)

Guidance literature:

sodium nonanoate; With chloroformic acid ethyl ester; In tetrahydrofuran; at 20 ℃; for 0.25h;

phenylzinc iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; at 70 ℃; for 14h;

DOI:10.1021/ol035801w

upstream raw materials:

Nonanoyl chloride

1-phenylnonan-1-ol

octylmagnesium bromide

benzonitrile

Downstream raw materials:

n-nonylbenzene

3-hydroxy-3-phenyl-undecanoic acid

6-Phenyl-n-tetradecanol-⁽⁶⁾

1-phenylnonan-1-amine