2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide

Base Information Edit

Chemical Name:2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide
CAS No.:5908-40-7
Molecular Formula:C22H23N3O2S
Molecular Weight:130.262
Hs Code.:2931900090
DSSTox Substance ID:DTXSID10360001
Wikidata:Q82141484
Mol file:5908-40-7.mol

Synonyms:5908-40-7;2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide;DTXSID10360001

Suppliers and Price of 2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide

Supply Marketing:Edit

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

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Chemical Property of 2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide Edit

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：94.03000
Density:1.236g/cm³
LogP:4.87940
XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:393.15109816
Heavy Atom Count:28
Complexity:504

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Canonical SMILES:CCCN(CC(=O)NC1=NC(=CS1)C2=CC=CC=C2)C(=O)CC3=CC=CC=C3
Physical properties Clear liquid; bp 74 °C/96 mmHg; d 0.8274 g cm?3 (26 °C), n26/D 1.4188.
Uses Trimethylsilylacetone reacts with Grignard or organolithium reagents to provide, after elimination, 2-substituted 2-propenes; in combination with fluoride ion, gives chemistry of the corresponding enolate ion; can direct electrophilic substitution to either side of the carbonyl group, participating in (but not limited to) reactions: Preparation of 2-substituted α-Alkenes, Reaction with Electrophiles, Reaction with Fluoride Ion, Reaction with Strong Bases, etc.

Technology Process of 2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide

There total 9 articles about 2-[(2-phenylacetyl)-propyl-amino]-N-(4-phenyl-1,3-thiazol-2-yl)acetamide 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: 80.0%