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Ethyl 3-(naphthalen-2-yl)propanoate

Base Information
  • Chemical Name:Ethyl 3-(naphthalen-2-yl)propanoate
  • CAS No.:112598-96-6
  • Molecular Formula:C15H16 O2
  • Molecular Weight:228.291
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60554433
  • Nikkaji Number:J2.313.990A
  • Wikidata:Q82435422
  • Mol file:112598-96-6.mol
Ethyl 3-(naphthalen-2-yl)propanoate

Synonyms:112598-96-6;ethyl 3-(naphthalen-2-yl)propanoate;ethyl 3-naphthalen-2-ylpropanoate;3-NAPHTHALEN-2-YL-PROPIONIC ACID ETHYL ESTER;SCHEMBL2385413;ethyl 3-(2-naphthyl)propionate;DTXSID60554433;BXSIHFSJIKHCNZ-UHFFFAOYSA-N;AKOS010486199

Suppliers and Price of Ethyl 3-(naphthalen-2-yl)propanoate
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
  • American Custom Chemicals Corporation
  • 3-NAPHTHALEN-2-YL-PROPIONIC ACID ETHYL ESTER 95.00%
  • 5MG
  • $ 495.08
Total 4 raw suppliers
Chemical Property of Ethyl 3-(naphthalen-2-yl)propanoate
Chemical Property:
  • PSA:26.30000 
  • LogP:3.33550 
  • XLogP3:4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:228.115029749
  • Heavy Atom Count:17
  • Complexity:249
Purity/Quality:

98%min *data from raw suppliers

3-NAPHTHALEN-2-YL-PROPIONIC ACID ETHYL ESTER 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)CCC1=CC2=CC=CC=C2C=C1
Technology Process of Ethyl 3-(naphthalen-2-yl)propanoate

There total 10 articles about Ethyl 3-(naphthalen-2-yl)propanoate 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:
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; Temperature; Time;
Guidance literature:
With borane-ammonia complex; copper(I)hydroxide/N-heterocyclic carbene complex; In tetrahydrofuran; at 50 ℃; for 16h; Schlenk technique; Inert atmosphere;
DOI:10.1039/c6cc09067b
Guidance literature:
acrylaldehyde diethyl acetal; 2-bromonaphthalene; With C16H18Cl2N2O4Pd2; potassium chloride; tetrabutylammonium acetate; potassium carbonate; In N,N-dimethyl acetamide; at 120 ℃; for 3.5h;
With hydrogenchloride; In water; ethyl acetate; at 20 ℃; chemoselective reaction;
DOI:10.1002/ejoc.200800047
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