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1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER

Base Information
  • Chemical Name:1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER
  • CAS No.:62677-71-8
  • Molecular Formula:C14H16O2
  • Molecular Weight:216.28
  • Hs Code.:
  • Mol file:62677-71-8.mol
1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER

Synonyms:

Suppliers and Price of 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER
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
  • 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER 95.00%
  • 5MG
  • $ 497.13
Total 6 raw suppliers
Chemical Property of 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER
Chemical Property:
  • Vapor Pressure:8.94E-05mmHg at 25°C 
  • Boiling Point:339.9oC at 760 mmHg 
  • Flash Point:202.1oC 
  • PSA:26.30000 
  • Density:1.138g/cm3 
  • LogP:2.96940 
Purity/Quality:

97% *data from raw suppliers

1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER

There total 5 articles about 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLIDINE ACETATIC ACID ETHYL ESTER 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:
diethoxyphosphoryl-acetic acid ethyl ester; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.25h; Inert atmosphere;
3,4-dihydronaphthalene-1(2H)-one; In tetrahydrofuran; for 16h; Inert atmosphere; Reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: 80 percent / zinc, iodine / tetrahydrofuran / 3.5 h / Heating
2: P2O5 / benzene / 2 h / Heating
With iodine; phosphorus pentoxide; zinc; In tetrahydrofuran; benzene;
DOI:10.1021/ja00267a036
Guidance literature:
With phosphorus pentoxide; In benzene; for 2h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Heating;
DOI:10.1021/ja00267a036
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