(2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide

Base Information

Chemical Name:(2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide
CAS No.:244239-94-9
Molecular Formula:C₁₀H₁₁NO₃
Molecular Weight:193.202
Hs Code.:
DSSTox Substance ID:DTXSID601197254

Synonyms:(2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide;DTXSID601197254;244239-94-9

Suppliers and Price of (2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of (2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:193.07389321
Heavy Atom Count:14
Complexity:231

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1C(O1)C(=O)NC2=CC=CC=C2O
Isomeric SMILES:C[C@@H]1[C@@H](O1)C(=O)NC2=CC=CC=C2O

Technology Process of (2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide

There total 1 articles about (2R,3R)-N-(2-Hydroxyphenyl)-3-methyl-2-oxiranecarboxamide 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: 48.0%

: 84823-47-2
(2R,3R)-potassium 2,3-epoxybutyrate

: 95-55-6
2-amino-phenol

: 244239-94-9
(2R,3R)-3-Methyl-oxirane-2-carboxylic acid (2-hydroxy-phenyl)-amide

Guidance literature:: (2R,3R)-potassium 2,3-epoxybutyrate; With 4-methyl-morpholine; isobutyl chloroformate; In tetrahydrofuran; at 0 ℃; for 1h;

2-amino-phenol; In tetrahydrofuran; at 20 ℃; for 20h;
DOI:10.1016/S0040-4020(99)00488-3