Boc-L-homophenylalanine

Base Information Edit

Chemical Name:Boc-L-homophenylalanine
CAS No.:100564-78-1
Molecular Formula:C₁₅H₂₁NO₄
Molecular Weight:279.336
Hs Code.:29242990
European Community (EC) Number:692-740-1
DSSTox Substance ID:DTXSID10427007
Nikkaji Number:J499.099D
Wikidata:Q72449511
Mol file:100564-78-1.mol

Synonyms:Boc-L-homophenylalanine;100564-78-1;Boc-Homophe-OH;Boc-L-Homo-Phe;(S)-2-((tert-Butoxycarbonyl)amino)-4-phenylbutanoic acid;BOC-HOPHE-OH;Boc-homophenylalanine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutanoic acid;BOC-HFE-OH;N-boc-L-homophenylalanine;N-BOC-(L)-HOMOPHENYLALANINE;(S)-2-(TERT-BUTOXYCARBONYLAMINO)-4-PHENYLBUTANOIC ACID;Boc-D-Homophe-OH;MFCD00076904;(S)-2-(BOC-AMINO)-4-PHENYL-BUTYRIC ACID;N-Boc-D-Homophe-OH;N-Boc-Homophenylalanine;Boc-(L)-homophenylalanine;Boc-3-Benzyl-L-Ala-OH;BOC-D-HOMOPHENYL-ALA;SCHEMBL181775;DTXSID10427007;MCODLPJUFHPVQP-LBPRGKRZSA-N;BCP09717;CS-D1787;HY-I0773;AKOS015889771;AC-9057;AC-9058;CS-O-11252;Boc-Homophe-OH, >=98.0% (TLC);N-(t-butoxycarbonyl)-L-homophenylalanine;AS-15600;(S)-2-(Boc-amino)-4-phenylbutyric acid;N-(tert-Butoxycarbonyl)-L-homophenylalanine;AM20050371;B4356;EN300-160093;A800236;(S)-2-tert-butoxycarbonylamino-4-phenylbutyric acid;J-300428;J-640376;(S)-N-t-butoxycarbonyl-2-amino-4-phenylbutyric acid;(S)-2-((tert-Butoxycarbonyl)amino)-4-phenylbutanoicacid;(S)-2-(tert-Butoxycarbonylamino)-4-phenylbutyric Acid;(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoic acid;(S)-2-(N-(tert-butoxycarbonyl)amino)-4-phenylbutanoic acid;(S)-2-TERT-BUTOXYCARBONYLAMINO-4-PHENYL-BUTYRIC ACID;(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-4-phenylbutanoic acid;(2S)-2-(tert-butoxycarbonylamino)-4-phenyl-butanoic acid;Benzenebutanoic acid, alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-, (alphaS)-

Suppliers and Price of Boc-L-homophenylalanine

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

Usbiological
Boc-L-homophenylalanine
2g
$ 333.00

Usbiological
Boc-L-homophenylalanine 99+%
1g
$ 159.00

TRC
N-Boc-L-homophenylalanine
5g
$ 65.00

TCI Chemical
N-(tert-Butoxycarbonyl)-L-homophenylalanine >98.0%(HPLC)(T)
5g
$ 42.00

TCI Chemical
N-(tert-Butoxycarbonyl)-L-homophenylalanine >98.0%(HPLC)(T)
1g
$ 14.00

SynQuest Laboratories
L-Homophenylalanine, N-Boc protected
25 g
$ 92.00

Sigma-Aldrich
Boc-Homophe-OH ≥98.0% (TLC)
1g
$ 130.00

Medical Isotopes, Inc.
(S)-2-((tert-Butoxycarbonyl)amino)-4-phenylbutanoicacid 98%
1 g
$ 310.00

Matrix Scientific
Boc-L-homophenylalanine
5g
$ 19.00

Matrix Scientific
Boc-L-homophenylalanine
25g
$ 59.00

Total 137 raw suppliers

Chemical Property of Boc-L-homophenylalanine Edit

Chemical Property:

Vapor Pressure:1.67E-08mmHg at 25°C
Melting Point:76-80 °C
Refractive Index:1.524
Boiling Point:439.6 °C at 760 mmHg
PKA:3.95±0.10(Predicted)
Flash Point:219.7 °C
PSA：75.63000
Density:1.139 g/cm³
LogP:2.98800
Storage Temp.:2-8°C
Solubility.:Soluble in methanol.
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:279.14705815
Heavy Atom Count:20
Complexity:329

Purity/Quality:

99% ^*data from raw suppliers

Boc-L-homophenylalanine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCC1=CC=CC=C1)C(=O)O
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CCC1=CC=CC=C1)C(=O)O
Uses N-Boc-L-homophenylalanine is a useful reagent for organic synthesis and other chemical processes. It is used in the preparation of piperidine-containing peptidyl proteasome inhibitors.

Technology Process of Boc-L-homophenylalanine

There total 63 articles about Boc-L-homophenylalanine 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: 98.0%