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(2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid

Base Information
  • Chemical Name:(2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid
  • CAS No.:62023-65-8
  • Molecular Formula:C15H21NO5
  • Molecular Weight:295.335
  • Hs Code.:2924299090
  • DSSTox Substance ID:DTXSID40444505
  • Nikkaji Number:J1.937.693A
  • Wikidata:Q82262656
  • Mol file:62023-65-8.mol
(2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid

Synonyms:62023-65-8;(2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid;N-Boc-(2S,3R)-2-hydroxy-3-amino-4-phenylbutanoic acid;(2S,3R)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoic acid;Boc-(2S,3R)-AHPA;(2S,3R)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutanoic acid;(2S,3R)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxy-4-phenylbutanoic acid;MFCD00057841;SCHEMBL825622;DTXSID40444505;AKOS016843855;AS-72743;CS-0134071;EN300-12447022;(2S,3R)-2-Hydroxy-3-(tert-butoxycarbonylamino)-4-phenylbutanoic acid;(2S,3R)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoicacid;(2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid, >=98.0% (TLC);(2S,3R)-3-(tert-butoxycarbonylamino)-2-hydroxy-4-phenylbutanoic acid

Suppliers and Price of (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid
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
  • AHH
  • N-Boc-(2S,3R)-2-hydroxy-3-amino-4-phenylbutanoicacid 98%
  • 0.5g
  • $ 305.00
  • Alfa Aesar
  • (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid, 97%
  • 250mg
  • $ 342.00
  • Alfa Aesar
  • (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid, 97%
  • 1g
  • $ 968.00
  • Alichem
  • (2S,3R)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoicacid
  • 1g
  • $ 646.84
  • American Custom Chemicals Corporation
  • N-BOC-(2S,3R)-2-HYDROXY-3-AMINO-4-PHENYLBUTANOIC ACID 95.00%
  • 1G
  • $ 1033.73
  • American Custom Chemicals Corporation
  • N-BOC-(2S,3R)-2-HYDROXY-3-AMINO-4-PHENYLBUTANOIC ACID 95.00%
  • 5G
  • $ 2656.50
  • American Custom Chemicals Corporation
  • N-BOC-(2S,3R)-2-HYDROXY-3-AMINO-4-PHENYLBUTANOIC ACID 95.00%
  • 1MG
  • $ 213.15
  • Chemenu
  • Boc-(2S,3R)-AHPA 95%
  • 1g
  • $ 729.00
  • Crysdot
  • (2S,3R)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoicacid 95+%
  • 1g
  • $ 772.00
  • Medical Isotopes, Inc.
  • N-Boc-(2S,3R)-2-hydroxy-3-amino-4-phenylbutanoicacid
  • 1 g
  • $ 695.00
Total 17 raw suppliers
Chemical Property of (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid
Chemical Property:
  • Boiling Point:499.1±45.0 °C(Predicted) 
  • PKA:3.57±0.17(Predicted) 
  • PSA:95.86000 
  • Density:1 +-.0.06 g/cm3(Predicted) 
  • LogP:1.95880 
  • Storage Temp.:−20°C 
  • Water Solubility.:Insoluble in water. Soluble in organic solvents. 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:295.14197277
  • Heavy Atom Count:21
  • Complexity:358
Purity/Quality:

98%,99%, *data from raw suppliers

N-Boc-(2S,3R)-2-hydroxy-3-amino-4-phenylbutanoicacid 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC(CC1=CC=CC=C1)C(C(=O)O)O
  • Isomeric SMILES:CC(C)(C)OC(=O)N[C@H](CC1=CC=CC=C1)[C@@H](C(=O)O)O
  • Uses (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid, is used as a novel protected amino acid for the preparation of bestatin and analogs.
Technology Process of (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid

There total 44 articles about (2S,3R)-3-(Boc-amino)-2-hydroxy-4-phenylbutyric acid 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 potassium carbonate; In tetrahydrofuran; water; at 0 - 20 ℃; for 1h;
Guidance literature:
Boc-D-Phe-OH; With sodium hydrogensulfite; In water; ethyl acetate; for 10h;
sodium cyanide; In water; ethyl acetate; at 20 ℃;
di-tert-butyl dicarbonate;
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