(4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol

Base Information

Chemical Name:(4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol
CAS No.:51594-33-3
Molecular Formula:C12H15NO2
Molecular Weight:205.257
Hs Code.:2934999090
European Community (EC) Number:637-106-7
Nikkaji Number:J9.133B
Wikidata:Q76416520
ChEMBL ID:CHEMBL2374808
Mol file:51594-33-3.mol

Synonyms:(4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol;51594-33-3;(2-Ethyl-5-phenyl-4,5-dihydro-1,3-oxazol-4-yl)methanol #;CHEMBL2374808;GZOYBTRDWOUZTG-JQWIXIFHSA-N;(4S)-2-Ethyl-5alpha-phenyl-2-oxazoline-4beta-methanol;[(4S,5S)-2-ethyl-5-phenyl-4,5-dihydro-1,3-oxazol-4-yl]methanol

Suppliers and Price of (4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol

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

TRC
(4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol
10mg
$ 45.00

American Custom Chemicals Corporation
(4S,5S)-(-)-2-ETHYL-5-PHENYL-2-OXAZOLINE-4-METHANOL 95.00%
5MG
$ 504.12

Total 1 raw suppliers

Chemical Property of (4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol

Chemical Property:

PSA：41.82000
LogP:1.36290
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:205.110278721
Heavy Atom Count:15
Complexity:234

Purity/Quality:: (4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=NC(C(O1)C2=CC=CC=C2)CO
Isomeric SMILES:CCC1=N[C@H]([C@@H](O1)C2=CC=CC=C2)CO

Technology Process of (4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol

There total 3 articles about (4S,5S)-(-)-2-Ethyl-5-phenyl-2-oxazoline-4-methanol 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: 30.0%

: 130007-66-8
R-(-)-2-(4-isobutyl-phenyl)-2-hydroxyethane

: 51594-33-3,412308-66-8
(4S,5S)-(-)-2-ethyl-4-hydroxymethyl-5-phenyl-2-oxazoline

Guidance literature:

Reference yield:

: 28143-91-1
(1S,2S)-2-amino-1-phenyl-1,3-diol

: 79-05-0
Propionamid

: 51594-33-3,412308-66-8
(4S,5S)-(-)-2-ethyl-4-hydroxymethyl-5-phenyl-2-oxazoline

Guidance literature:: With triethyloxonium fluoroborate; Yield given. Multistep reaction; 1.) 1,2-dichloroethane, RT, 20 h, 2.) 1,2-dichloroethane, reflux, 18 h;