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Benzyl octahydro-1H-indole-2-carboxylate hydrochloride

Base Information
  • Chemical Name:Benzyl octahydro-1H-indole-2-carboxylate hydrochloride
  • CAS No.:82717-97-3
  • Molecular Formula:C16H21NO2.ClH
  • Molecular Weight:295.809
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60601153
Benzyl octahydro-1H-indole-2-carboxylate hydrochloride

Synonyms:82717-97-3;benzyloctahydroindole-2-carboxylate hydrochloride;BENZYL OCTAHYDRO-1H-INDOLE-2-CARBOXYLATE HYDROCHLORIDE;Octahydroindoline-2-carboxylic Acid Benzyl Ester Hydrochloride;benzyl 2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylate;hydrochloride;2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylic acid (phenylmethyl) ester hydrochloride;WOXVBEWLLZBVSX-UHFFFAOYSA-N;SCHEMBL5549535;DTXSID60601153;DA-35037;EN300-270188;A808399;BENZYLOCTAHYDRO-1H-INDOLE-2-CARBOXYLATEHYDROCHLORIDE;octahydroindole-2-carboxylic acid benzyl ester hydrochloride;Benzyl octahydro-1H-indole-2-carboxylate--hydrogen chloride (1/1);benzyl 2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylate,hydrochloride

Suppliers and Price of Benzyl octahydro-1H-indole-2-carboxylate hydrochloride
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
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Total 3 raw suppliers
Chemical Property of Benzyl octahydro-1H-indole-2-carboxylate hydrochloride
Chemical Property:
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:295.1339066
  • Heavy Atom Count:20
  • Complexity:312
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC2C(C1)CC(N2)C(=O)OCC3=CC=CC=C3.Cl
Technology Process of Benzyl octahydro-1H-indole-2-carboxylate hydrochloride

There total 2 articles about Benzyl octahydro-1H-indole-2-carboxylate hydrochloride 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:
Cis,exo-perhydroindole-2-L-carboxylic acid hydrochloride; benzyl alcohol; toluene-4-sulfonic acid; In toluene; for 3h;
With sodium hydroxide; In water; toluene; pH=11;
With hydrogenchloride; In methanol;
Guidance literature:
octahydroindole-2-carboxylic acid benzyl ester hydrochloride; With sodium hydroxide; In water; for 1h;
With O,O'-dibenzoyl-L-tartaric acid; In methanol; for 1h; Resolution of racemate;
With hydrogenchloride; sodium hydroxide; more than 3 stages;
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