9-Phenyl-1-nonanol

Base Information

• Chemical Name: 9-Phenyl-1-nonanol
• CAS No.: 3208-26-2
• Molecular Formula: C15H24O
• Molecular Weight: 220.355
• Hs Code.: 2906299090
• DSSTox Substance ID: DTXSID00427435
• Wikidata: Q82240091
• Mol file: 3208-26-2.mol

Synonyms:9-phenylnonan-1-ol;9-PHENYL-1-NONANOL;3208-26-2;Benzenenonanol;9-Phenyl-n-nonanol;9-(phenyl)-nonan-1-ol;SCHEMBL1007095;DTXSID00427435;FT-0621685;A875716;J-018626

Chemical Property of 9-Phenyl-1-nonanol

Chemical Property:

• Vapor Pressure: 7.68E-05mmHg at 25°C
• Refractive Index: 1.5030
• Boiling Point: 328.4 °C at 760 mmHg
• PKA: 15.20±0.10(Predicted)
• Flash Point: 123.8 °C
• PSA: 20.23000
• Density: 0.936 g/cm³
• LogP: 3.95210
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 220.182715385
• Heavy Atom Count: 16
• Complexity: 138

Purity/Quality:

98%Min ^*data from raw suppliers

9-PHENYL-1-NONANOL 95.00% ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCCCCCCCCO

Technology Process of 9-Phenyl-1-nonanol

There total 23 articles about 9-Phenyl-1-nonanol 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%

2-(9-Phenyl-nonyloxy)-tetrahydro-pyran (117806-56-1) → 9-phenyl-1-hydroxynonane (3208-26-2)

Guidance literature:

hydrogenchloride; In methanol; for 1h; Heating;

DOI:10.1016/S0040-4039(98)00297-4

Reference yield: 95.0%

9-phenylnonanoic acid methyl ester (24197-55-5) → 9-phenyl-1-hydroxynonane (3208-26-2)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran;

DOI:10.3987/COM-95-7293

Reference yield: 84.0%

9-phenylnonanoic acid (16269-06-0) → 9-phenyl-1-hydroxynonane (3208-26-2)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; 1.) RT, 1.5 h, 2.) reflux, 1h.;

upstream raw materials:

1-(α-furyl)-5-phenylpenta-1,4-dien-3-one

9-phenylnonanoic acid

9-phenylnonanoic acid methyl ester

2-(9-Phenyl-nonyloxy)-tetrahydro-pyran

Downstream raw materials:

9-phenyl-1-bromononane

9-phenylnonanoic acid

9-(phenyl)-nonan-1-al

Refernces

• 1、 Yang, Lin-Feng,Shimadate, Yuna,Kato, Atsushi,Li, Yi-Xian,Jia, Yue-Mei,Fleet, George W. J.,Yu, Chu-Yi. "Synthesis and glycosidase inhibition of: N-substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM)". . p. 999 - 1011. Retrieved 2020/02/15.
• 2、 Pahl, Axel,Wartchow, Rudolf,Meyer, Hartmut H.. "Syntheses of (-)-(2R,3R,6S)-irnigaine and (+)-(2R,3R,6S)-N- methylirnigaine". . p. 2095 - 2096. Retrieved 2007/10/03.