Boc-4-amino-L-phenylalanine

Base Information Edit

Chemical Name:Boc-4-amino-L-phenylalanine
CAS No.:55533-24-9
Molecular Formula:C14H20N2O4
Molecular Weight:280.324
Hs Code.:29242990
European Community (EC) Number:811-732-2
DSSTox Substance ID:DTXSID30375793
Nikkaji Number:J1.687.639I
Wikidata:Q72448329
Mol file:55533-24-9.mol

Synonyms:55533-24-9;BOC-4-AMINO-L-PHENYLALANINE;Boc-Phe(4-NH2)-OH;4-Amino-N-Boc-L-phenylalanine;Boc-L-4-aminophenylalanine;(S)-3-(4-Aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid;4-Amino-N-(tert-butoxycarbonyl)-L-phenylalanine;(2S)-3-(4-aminophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;MFCD00038139;Boc-p-amino-Phe-OH;Boc-4-Amino-Phe-OH;(2S)-3-(4-aminophenyl)-2-(tert-butoxycarbonylamino)propanoic acid;boc-4-aminophenylalanine;Boc-p-amino-L-Phe-OH;Boc-4-Amino-L-Phe-OH;Boc-para-aminophenylalanine;N-Boc 4-aminophenylalanine;N-Boc-4-aminophenylalanine;Boc-p-amino-L-phenylalanine;SCHEMBL376103;DTXSID30375793;NDMVQEZKACRLDP-NSHDSACASA-N;(2S)-3-(4-aminophenyl)-2-{[(tert-butoxy)carbonyl]amino}propanoic acid;AKOS015841395;AC-9059;CS-W007620;HY-W007620;(2S)-3-(4-aminophenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid;AS-18417;BP-30225;PD196489;AM20050367;N-tert-Butoxycarbonyl-4-amino-L-phenylalanine;M01307;O10217;Boc-Phe(4-NH2)-OH, >=98.0% (HPLC);EN300-6497686;A830693;Boc-4-Amino-L-phenylalanine Boc-Phe(4-NH2)-OH;N-alpha-t-Butoxycarbonyl-DL-4-amino-phenylalanine;J-519906;4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-1-phenylalanine;4-Amino-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine;(S)-3-(4-aminophenyl)-2-(tert-butoxycarbonylamino)propanoic acid;(2S)-3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Suppliers and Price of Boc-4-amino-L-phenylalanine

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
Boc-4-Amino-L-phenylalanine
1000mg
$ 160.00

TCI Chemical
4-Amino-N-(tert-butoxycarbonyl)-L-phenylalanine >96.0%(HPLC)(T)
1g
$ 80.00

TCI Chemical
4-Amino-N-(tert-butoxycarbonyl)-L-phenylalanine >96.0%(HPLC)(T)
5g
$ 272.00

SynQuest Laboratories
4-Amino-L-phenylalanine, N-Boc protected
25 g
$ 266.00

SynQuest Laboratories
4-Amino-L-phenylalanine, N-Boc protected
5 g
$ 79.00

SynQuest Laboratories
4-Amino-L-phenylalanine, N-Boc protected
10 g
$ 122.00

Sigma-Aldrich
Boc-Phe(4-NH2)-OH ≥98.0% (HPLC)
500mg
$ 104.00

Matrix Scientific
Boc-4-amino-L-phenylalanine
5g
$ 300.00

Matrix Scientific
Boc-4-amino-L-phenylalanine
1g
$ 72.00

Iris Biotech GmbH
Boc-L-Phe(4-NH2)-OH
1 g
$ 243.00

Total 105 raw suppliers

Chemical Property of Boc-4-amino-L-phenylalanine Edit

Chemical Property:

Melting Point:124-126℃
Boiling Point:484.9 °C at 760 mmHg
PKA:3.74±0.10(Predicted)
Flash Point:247 °C
PSA：101.65000
Density:1.213 g/cm³
LogP:2.76130
Storage Temp.:-15°C
XLogP3:1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:280.14230712
Heavy Atom Count:20
Complexity:344

Purity/Quality:

99% ^*data from raw suppliers

Boc-4-Amino-L-phenylalanine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-28

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)N)C(=O)O
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)N)C(=O)O
Uses Boc-4-Amino-L-phenylalanine is an intermediate used in the synthesis of biotinylated amino acids.

Technology Process of Boc-4-amino-L-phenylalanine

There total 15 articles about Boc-4-amino-L-phenylalanine 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:

Reference yield: 96.0%

: 33305-77-0
Boc-Phe(p-NO₂)-OH

: 55533-24-9,164332-89-2
L-N-tert-butoxycarbonyl-p-aminophenylalanine

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; Inert atmosphere;
DOI:10.1021/mp2001878

Reference yield: 80.0%

: 33305-77-0,86937-80-6,105453-25-6,61280-75-9
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-nitrophenyl)propanoic acid

: 55533-24-9,164332-89-2
(2R)-3-(4-aminophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 24h; under 2585.74 Torr;
DOI:10.1016/j.ejmech.2006.03.021