alpha-(Phenethylimino)-O-cresol

Base Information

• Chemical Name: alpha-(Phenethylimino)-O-cresol
• CAS No.: 49792-36-1
• Molecular Formula: C15H15NO
• Molecular Weight: 225.29
• European Community (EC) Number: 666-333-4
• DSSTox Substance ID: DTXSID60425619
• Nikkaji Number: J658.033E
• Mol file: 49792-36-1.mol

Synonyms:AC1OAAUQ;CBDivE_014222;49792-36-1;ALPHA-(PHENETHYLIMINO)-O-CRESOL;DTXSID60425619;N-salicylidene-2-phenylethylamine;STL577069;AKOS024336859;2-[[(2-Phenylethyl)imino]methyl]phenol;EU-0050855;2-{(E)-[(2-phenylethyl)imino]methyl}phenol

Chemical Property of alpha-(Phenethylimino)-O-cresol

Chemical Property:

• PSA: 29.10000
• LogP: 2.78860
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 225.115364102
• Heavy Atom Count: 17
• Complexity: 233

Purity/Quality:

ALPHA-(PHENETHYLIMINO)-O-CRESOL Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCN=CC2=CC=CC=C2O

Technology Process of alpha-(Phenethylimino)-O-cresol

There total 1 articles about alpha-(Phenethylimino)-O-cresol 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: 86.0%

salicylaldehyde (90-02-8) + phenethylamine (64-04-0) → 2-[[(2-phenylethyl)imino]methyl]phenol (49792-36-1)

Guidance literature:

In neat (no solvent); at 120 ℃; Inert atmosphere;

DOI:10.1039/c3dt32183e

Reference yield: 75.0%

2-[[(2-phenylethyl)imino]methyl]phenol (49792-36-1) + tetrabutylammonium tricyano(hydrotris(3,5-dimethylpyrazol-1-yl)borate)ferrate(III) (1258869-01-0) + manganese(III) triacetate dihydrate (19513-05-4) → [Mn(2-[[(2-phenylethyl)imino]methyl]phenol)2Fe(hydrotris(3,5-dimethylpyrazol-1-yl)borate)(CN)3]n

Guidance literature:

In methanol; acetone; at 60 ℃; for 12h;

DOI:10.1002/zaac.201500214

Reference yield:

2-[[(2-phenylethyl)imino]methyl]phenol (49792-36-1) → N-2-hydroxyphenylmethyl-2-phenylethylamine

Guidance literature:

With sodium tetrahydroborate; In methanol; dichloromethane; at 5 - 20 ℃; for 22h;

DOI:10.1016/j.molstruc.2016.04.079

upstream raw materials:

salicylaldehyde

phenethylamine

Downstream raw materials:

chlorobis(N-(2-phenylethyl)salicylideniminato)iron(III)

bis(N-β-phenylethyl-salicylaldiminato)beryllium(II)