Methyl 5-(1-naphthyl)-5-oxopentanoate

Base Information

Chemical Name:Methyl 5-(1-naphthyl)-5-oxopentanoate
CAS No.:13672-44-1
Molecular Formula:C₁₆H₁₆O₃
Molecular Weight:256.301
Hs Code.:
DSSTox Substance ID:DTXSID901288961

Synonyms:methyl 5-(1-naphthyl)-5-oxopentanoate;SCHEMBL26597083;DTXSID901288961;Methyl delta-oxo-1-naphthalenepentanoate;13672-44-1;methyl 5-naphthalen-1-yl-5-oxopentanoate;methyl 5-(naphthalen-1-yl)-5-oxopentanoate

Suppliers and Price of Methyl 5-(1-naphthyl)-5-oxopentanoate

Supply Marketing:

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

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Chemical Property of Methyl 5-(1-naphthyl)-5-oxopentanoate

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:256.109944368
Heavy Atom Count:19
Complexity:324

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)CCCC(=O)C1=CC=CC2=CC=CC=C21

Technology Process of Methyl 5-(1-naphthyl)-5-oxopentanoate

There total 1 articles about Methyl 5-(1-naphthyl)-5-oxopentanoate 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%

: 53441-73-9,53441-90-0,125331-38-6
phenyl-N-(1-naphthylethylidene)methanamine

: 292638-85-8,9003-21-8,96-33-3
acrylic acid methyl ester

: 3-[1-(1-benzyliminoethyl)-naphthalen-2-yl]propionic acid methyl ester

: 13672-44-1
5-naphthalen-1-yl-5-oxopentanoic acid methyl ester

Guidance literature:: phenyl-N-(1-naphthylethylidene)methanamine; acrylic acid methyl ester; With Wilkinson's catalyst; In toluene; at 150 ℃; for 2h;

With hydrogenchloride; In toluene; at 20 ℃;
DOI:10.1021/ol048095n

Reference yield:

: 64-17-5
ethanol

: 13246-50-9
benzylchlorotriphenylphosphorane

: 13672-44-1
5-naphthalen-1-yl-5-oxopentanoic acid methyl ester

: 110971-51-2,110971-68-1
ethyl 5-(1-naphthyl)-6-phenyl-5-hexanoate

: 110971-68-1
ethyl 5-(1-naphthyl)-6-phenyl-5-hexanoate

Guidance literature:: With sodium ethanolate; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) 1 h, 2.) reflux, 72 h;
DOI:10.1021/jo00234a013