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ethyl (3S)-piperidine-3-carboxylate

Base Information Edit
  • Chemical Name:ethyl (3S)-piperidine-3-carboxylate
  • CAS No.:37675-18-6
  • Molecular Formula:C8H15NO2
  • Molecular Weight:157.213
  • Hs Code.:29339900
  • European Community (EC) Number:609-464-4
  • DSSTox Substance ID:DTXSID10191110
  • Nikkaji Number:J231.782F
  • Wikidata:Q72476879
  • Mol file:37675-18-6.mol
ethyl (3S)-piperidine-3-carboxylate

Synonyms:37675-18-6;(S)-Ethyl piperidine-3-carboxylate;ethyl (3S)-piperidine-3-carboxylate;Ethyl (S)-nipecotate;(S)-(+)-Nipecotic Acid Ethyl Ester;(S)-Ethyl nipecotate;Ethyl (S)-piperidine-3-carboxylate;3-Piperidinecarboxylic acid, ethyl ester, (3S)-;MFCD00792499;(S)-PIPERIDINE-3-CARBOXYLIC ACID ETHYL ESTER;(S)-Nipecotic Acid ethyl Ester;(S)-(+)-ETHYL NIPECOTATE;ethyl(3s)-piperidine-3-carboxylate;(s)-(+)-ethylnipecotate;Ethyl (S)-(+)-Nipecotate;SCHEMBL134525;DTXSID10191110;(S)-Ethylpiperidine-3-carboxylate;ethyl(S)-piperidine-3-carboxylate;BCP13769;CS-CU-00012;ethyl (3S)-3-piperidinecarboxylate;ethyl (3S)-3-piperidine carboxylate;(S)-(-)-nipecotic acid ethyl ester;AKOS005257667;(|S|)-Ethyl piperidine-3-carboxylate;(S)-(+)-nipecotic acid, ethyl ester;CS-W010912;Ethyl (S)-(+)-3-Piperidinecarboxylate;AS-15837;(S)-Ethyl piperidine-3-carboxylate, 97%;3beta-Piperidinecarboxylic acid ethyl ester;A6434;AM20100005;N0679;EN300-83429;(S)-(+)-3-Piperidinecarboxylic Acid Ethyl Ester

Suppliers and Price of ethyl (3S)-piperidine-3-carboxylate
Supply Marketing:Edit
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
  • TRC
  • (S)-Ethyl piperidine-3-carboxylate
  • 100mg
  • $ 60.00
  • TRC
  • (S)-Ethyl piperidine-3-carboxylate
  • 500mg
  • $ 75.00
  • TCI Chemical
  • Ethyl (S)-(+)-3-Piperidinecarboxylate >98.0%(GC)(T)
  • 5g
  • $ 108.00
  • TCI Chemical
  • Ethyl (S)-(+)-3-Piperidinecarboxylate >98.0%(GC)(T)
  • 25g
  • $ 382.00
  • SynQuest Laboratories
  • Ethyl (3S)-piperidine-3-carboxylate
  • 5 g
  • $ 200.00
  • SynQuest Laboratories
  • Ethyl (3S)-piperidine-3-carboxylate
  • 1 g
  • $ 72.00
  • Sigma-Aldrich
  • (S)-Ethyl piperidine-3-carboxylate 97%
  • 1g
  • $ 93.80
  • Frontier Specialty Chemicals
  • Ethyl (S)-(+)-3-Piperidinecarboxylate 98%
  • 1g
  • $ 85.00
  • Frontier Specialty Chemicals
  • Ethyl (S)-(+)-3-Piperidinecarboxylate 98%
  • 5g
  • $ 339.00
  • Crysdot
  • (S)-Ethyl piperidine-3-carboxylate 97%
  • 100g
  • $ 189.00
Total 129 raw suppliers
Chemical Property of ethyl (3S)-piperidine-3-carboxylate Edit
Chemical Property:
  • Appearance/Colour:liquid 
  • Vapor Pressure:0.042mmHg at 25°C 
  • Refractive Index:n20/D 1.471 
  • Boiling Point:238.6 °C at 760 mmHg 
  • PKA:9.35±0.10(Predicted) 
  • Flash Point:90.6 °C 
  • PSA:38.33000 
  • Density:1.003 g/cm3 
  • LogP:0.87790 
  • Storage Temp.:Refrigerator 
  • Sensitive.:Light, Air & Moisture Sensitive 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:157.110278721
  • Heavy Atom Count:11
  • Complexity:136
Purity/Quality:

99%min *data from raw suppliers

(S)-Ethyl piperidine-3-carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38-41 
  • Safety Statements: 26-36/37/39-39-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C1CCCNC1
  • Isomeric SMILES:CCOC(=O)[C@H]1CCCNC1
  • Uses Reactant for synthesis of:DPP-4 inhibitorsJAK2 inhibitorsSerotonin and noradrenaline reuptake inhibitorsHuman tryptase inhibitorsAnti-thrombotic nicecotamidesReactive for oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H bond functionalization
Technology Process of ethyl (3S)-piperidine-3-carboxylate

There total 14 articles about ethyl (3S)-piperidine-3-carboxylate 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 sodium hydroxide; In water; at 0 ℃;
Guidance literature:
With sodium hydroxide; In water;
Guidance literature:
Ethyl nipecotate; With L-Tartaric acid;
With potassium carbonate;
DOI:10.1016/j.tetlet.2004.01.157
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