2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol

Base Information

Chemical Name:2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol
CAS No.:23175-16-8
Molecular Formula:C11H17 N O2
Molecular Weight:195.261
Hs Code.:2922199090
European Community (EC) Number:607-204-4
DSSTox Substance ID:DTXSID90405388
Nikkaji Number:J1.647.531I
Mol file:23175-16-8.mol

Synonyms:23175-16-8;2-[(2-hydroxyethyl)methylamino]-1-phenylethanol;2-[2-hydroxyethyl(methyl)amino]-1-phenylethanol;2-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-1-PHENYL-ETHANOL;HMS1718O03;SCHEMBL5878741;2-[(2-HYDROXYETHYL)(METHYL)AMINO]-1-PHENYLETHANOL;DTXSID90405388;AKOS001064689;AKOS017262081;Z31371712;2-[(2-Hydroxyethyl)(methyl)amino]-1-phenylethan-1-ol

Suppliers and Price of 2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol

Chemical Property:

PSA：43.70000
LogP:0.64410
XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:195.125928785
Heavy Atom Count:14
Complexity:146

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CCO)CC(C1=CC=CC=C1)O

Technology Process of 2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol

There total 2 articles about 2-[(2-Hydroxyethyl)methylamino]-1-phenylethanol 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: 88.0%

: 109-83-1
(2-hydroxyethyl)(methyl)amine

: 96-09-3
styrene oxide

: 23175-16-8
β-hydroxy-N-methyl-N-hydroxyethylphenylethylamine

Guidance literature:: at 130 ℃; for 24h;
DOI:10.1021/jm010566d

Reference yield:

: 23175-16-8
β-hydroxy-N-methyl-N-hydroxyethylphenylethylamine

Guidance literature:: 1-Phenyl-2-methylamino-ethanol (III-1) in Me. m. Ethylenoxid;

Reference yield: 95.0%

: 14103-74-3
bis(dimethylamino)dimethylgermane

: 85141-93-1
CH₃N(CH₂CH₂OH)CH(C₆H₅)CH₂OH

: 23175-16-8
β-hydroxy-N-methyl-N-hydroxyethylphenylethylamine

: 921595-29-1
[Ge(CH₃)2(CH₃N(CH₂CH₂O)CH₂CH(C₆H₅)O)]

: Ge⁽⁴⁺⁾*2CH₃^(1-)*CH₃N(CH₂CH₂O)CH₂CH(C₆H₅)O^(2-)=[Ge(CH₃)2(CH₃N(CH₂CH₂O)CH₂CH(C₆H₅)O)]

Guidance literature:: In toluene; byproducts: (CH3)2NH; (N2); using Schlenk techniques; heating of mixt. of MeN(CH2CH2OH)CH2CH(Ph)OH + MeN(CH2CH2OH)CH(Ph)CH2OH, Me2Ge(NMe2)2 and toluene at 70°Cfor 15 h; removal of all volatile materials under reduced pressure, drying in vac., elem. anal.; as mixt.;