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N-tert-Butyloxycarbonyl-dl-azidoalanine

Base Information Edit
  • Chemical Name:N-tert-Butyloxycarbonyl-dl-azidoalanine
  • CAS No.:108283-49-4
  • Molecular Formula:C8H14N4O4
  • Molecular Weight:230.224
  • Hs Code.:
  • UNII:UG8TQ789WL
  • DSSTox Substance ID:DTXSID70148483
  • Wikidata:Q83014024
  • Mol file:108283-49-4.mol
N-tert-Butyloxycarbonyl-dl-azidoalanine

Synonyms:CCRIS 1795;N-tert-Butyloxycarbonyl-dl-azidoalanine;UG8TQ789WL;UNII-UG8TQ789WL;N-Azido-N-((1,1-dimethylethoxy)carbonyl)-L-alanine;108283-49-4;L-Alanine, N-azido-N-((1,1-dimethylethoxy)carbonyl)-;(2S)-2-(Azido((tert-butoxy)carbonyl)amino)propanoic acid;2-(Azido((tert-butoxy)carbonyl)amino)propanoic acid, (2S)-;958802-96-5;Boc-azidoalanine;SCHEMBL873989;DTXSID70148483;NOAOACNYCMDXCJ-YFKPBYRVSA-N;XEA22554;LS-188961;Boc-L-aza-oh,boc-L-beta-azidoalanine,N-alpha-t-butyloxycarbonyl-3-azido-L-alanine,(S)-2-t-butyloxycarbonylamino-3-azidopropanoic acid cyclohexylamine

Suppliers and Price of N-tert-Butyloxycarbonyl-dl-azidoalanine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Chemical Property of N-tert-Butyloxycarbonyl-dl-azidoalanine Edit
Chemical Property:
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:230.10150494
  • Heavy Atom Count:16
  • Complexity:329
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C(=O)O)N(C(=O)OC(C)(C)C)N=[N+]=[N-]
  • Isomeric SMILES:C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)N=[N+]=[N-]
Technology Process of N-tert-Butyloxycarbonyl-dl-azidoalanine

There total 19 articles about N-tert-Butyloxycarbonyl-dl-azidoalanine 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 lithium hydroxide monohydrate; In tetrahydrofuran; water; at 0 ℃; for 1h;
DOI:10.1021/jacs.7b06144
Guidance literature:
With lithium hydroxide; In tetrahydrofuran; water; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1016/j.bmcl.2017.11.017
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