2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-

Base Information

Chemical Name:2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-
CAS No.:173220-67-2
Molecular Formula:C18H17NO2
Molecular Weight:279.338
Hs Code.:
DSSTox Substance ID:DTXSID101152267
Wikidata:Q105264070

Synonyms:173220-67-2;2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-;SB 204900;DTXSID101152267;AKOS040749410;(2S,3R)-N-Methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-2-oxiranecarboxamide

Suppliers and Price of 2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-

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 2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-

Chemical Property:

Vapor Pressure:2.27E-09mmHg at 25°C
Boiling Point:479.9°Cat760mmHg
Flash Point:244°C
Density:1.202g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:279.125928785
Heavy Atom Count:21
Complexity:381

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C=CC1=CC=CC=C1)C(=O)C2C(O2)C3=CC=CC=C3
Isomeric SMILES:CN(/C=C\C1=CC=CC=C1)C(=O)[C@@H]2[C@H](O2)C3=CC=CC=C3

Technology Process of 2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)-

There total 3 articles about 2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)- 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: 94.0%

: 1184725-15-2
C₁₇H₁₅NO₂

: 74-88-4
methyl iodide

: 173220-67-2
(2S,3R)-N-methyl-N-(Z)-styryl-3-phenyloxirane-2-carboxamide

Guidance literature:: C₁₇H₁₅NO₂; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h; Inert atmosphere;

methyl iodide; In N,N-dimethyl-formamide; at 0 ℃; for 2h; Inert atmosphere;
DOI:10.1039/b901965k

Reference yield:

: 588-73-8,1340-14-3
(Z)-β-bromostyrene

: 173220-67-2
(2S,3R)-N-methyl-N-(Z)-styryl-3-phenyloxirane-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; caesium carbonate; dimethylaminoacetic acid / 1,4-dioxane / Reflux

2: sodium hydride

With copper(l) iodide; dimethylaminoacetic acid; sodium hydride; caesium carbonate; In 1,4-dioxane;
DOI:10.1039/c4cc10327k

Reference yield:

: 1184725-14-1
(2S,3R)-3-phenyloxirane-2-carboxamide

: 173220-67-2
(2S,3R)-N-methyl-N-(Z)-styryl-3-phenyloxirane-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; caesium carbonate; dimethylaminoacetic acid / 1,4-dioxane / Reflux

2: sodium hydride

With copper(l) iodide; dimethylaminoacetic acid; sodium hydride; caesium carbonate; In 1,4-dioxane;
DOI:10.1039/c4cc10327k