2-(4-Methoxyphenoxy)propanoic acid, (-)-

Base Information

Chemical Name:2-(4-Methoxyphenoxy)propanoic acid, (-)-
CAS No.:4276-74-8
Molecular Formula:C10H12O4
Molecular Weight:196.203
Hs Code.:
UNII:7T1FBU2P6I
DSSTox Substance ID:DTXSID101278566
Nikkaji Number:J77.020E
Wikidata:Q27268809

Synonyms:Lactisole S-isomer;Lactisole, (S)-;Lactisole, (-)-;Lactisole S-isomer [MI];UNII-7T1FBU2P6I;7T1FBU2P6I;(S)-2-(4-Methoxyphenoxy)propionic acid;2-(4-Methoxyphenoxy)propanoic acid, (-)-;4276-74-8;Propanoic acid, 2-(4-methoxyphenoxy)-, (2S)-;(2S)-2-(4-methoxyphenoxy)propanoic acid;SCHEMBL5600662;DTXSID101278566;(-)-2-(4-methoxyphenoxy)propanoic acid;[S,(?)]-2-(p-Methoxyphenoxy)propionic acid;EN300-2124398;Q27268809

Suppliers and Price of 2-(4-Methoxyphenoxy)propanoic acid, (-)-

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 3 raw suppliers

Chemical Property of 2-(4-Methoxyphenoxy)propanoic acid, (-)-

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:196.07355886
Heavy Atom Count:14
Complexity:185

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C(=O)O)OC1=CC=C(C=C1)OC
Isomeric SMILES:C[C@@H](C(=O)O)OC1=CC=C(C=C1)OC

Technology Process of 2-(4-Methoxyphenoxy)propanoic acid, (-)-

There total 7 articles about 2-(4-Methoxyphenoxy)propanoic acid, (-)- 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: 82.0%

: methyl (2S)-2-(4-methoxyphenoxy)propanoate

: 4276-74-8,4276-73-7,4276-75-9
(S)-2-(4-nethoxyphenoxy)propionic acid

Guidance literature:: With potassium carbonate; In methanol; water; for 2h; Reflux;
DOI:10.1371/journal.pone.0213552

Reference yield: 80.0%

: 4276-74-8,4276-73-7,4276-75-9
(S)-2-(4-nethoxyphenoxy)propionic acid

Guidance literature:

Reference yield:

: 13794-15-5,4276-73-7,4276-75-9
2-(4-methoxyphenoxy)propanoic acid

: 4276-73-7,4276-75-9
2-(4-nethoxyphenoxy)propionic acid

: 4276-74-8,4276-73-7,4276-75-9
(S)-2-(4-nethoxyphenoxy)propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 6 h / 20 °C / Inert atmosphere

2: sodium carbonate; water / acetonitrile

With oxalyl dichloride; water; sodium carbonate; N,N-dimethyl-formamide; In dichloromethane; acetonitrile;
DOI:10.1002/ejoc.201800656