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5-Aminopentanal

Base Information
  • Chemical Name:5-Aminopentanal
  • CAS No.:14049-15-1
  • Molecular Formula:C5H11NO
  • Molecular Weight:101.148
  • Hs Code.:
  • UNII:7AC7RQZ8BZ
  • DSSTox Substance ID:DTXSID20332133
  • Nikkaji Number:J492.786I
  • Wikidata:Q27114159
  • Metabolomics Workbench ID:42109
  • ChEMBL ID:CHEMBL2261443
  • Mol file:14049-15-1.mol
5-Aminopentanal

Synonyms:5-Aminopentanal;Pentanal, 5-amino-;14049-15-1;5-Amino-pentanal;CHEBI:31130;5-Azanylpentanal;5-Aminovaleraldehyde;Valeraldehyde, 5-amino-;7AC7RQZ8BZ;SCHEMBL97690;CHEMBL2261443;DTXSID20332133;AKOS006337467;EN300-7491913;Q27114159

Suppliers and Price of 5-Aminopentanal
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The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of 5-Aminopentanal
Chemical Property:
  • XLogP3:-0.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:101.084063974
  • Heavy Atom Count:7
  • Complexity:45.3
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCN)CC=O
Technology Process of 5-Aminopentanal

There total 5 articles about 5-Aminopentanal 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 acridine orange; diamine oxidase from hog kidney; cucurbituril; at 37 ℃; pH=7.2; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1021/ja904165c
Guidance literature:
With nitrobenzene; Irradiation; also in presence of biacetyl and benzophenone;
Guidance literature:
Mechanism; Rate constant; Irradiation; reaction also in presence of biacetyl and benzophenone or O2;
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