220701
L-Phenylalanine ethyl ester hydrochloride
99%
Synonym(s):
(S)-Phenylalanine ethyl ester hydrochloride
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About This Item
Linear Formula:
C6H5CH2CH(NH2)COOC2H5 · HCl
CAS Number:
Molecular Weight:
229.70
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
221-673-9
MDL number:
Beilstein/REAXYS Number:
3657823
InChI key
FPFQPLFYTKMCHN-PPHPATTJSA-N
InChI
1S/C11H15NO2.ClH/c1-2-14-11(13)10(12)8-9-6-4-3-5-7-9;/h3-7,10H,2,8,12H2,1H3;1H/t10-;/m0./s1
SMILES string
Cl.CCOC(=O)[C@@H](N)Cc1ccccc1
assay
99%
optical activity
[α]20/D −7.8°, c = 2 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
155-156 °C (lit.)
application(s)
peptide synthesis
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Gayong Shim et al.
Nanotoxicology, 11(6), 762-770 (2017-07-08)
Poly-γ-glutamic acid (PGA), a major component of the bacterial capsule, is known to confer hydrophilicity to bacterial surfaces and protect bacteria from interactions with blood cells. We tested whether applying a bacteriomimetic surface coating of PGA modulates interactions of nanomaterials
João Albuquerque et al.
Scientific reports, 10(1), 6830-6830 (2020-04-24)
The amino acid requirements of high-production dairy cows represent a challenge to ensuring that their diet is supplied with available dietary resources, and thus supplementation with protected amino acids is necessary to increase their post-ruminal supply. Lysine is often the
Dongyoon Kim et al.
Biomaterials science, 8(4), 1106-1116 (2020-01-30)
In this study, we sought to design a bionanomaterial that could exert anticancer effects against primary tumors and protect against rechallenged tumors via photodynamic immunotherapy. As a biomaterial, we used an amphiphilic phenylalanine derivative of poly-gamma glutamic acid, which forms
Andreas J Reichert et al.
Protein engineering, design & selection : PEDS, 28(12), 553-565 (2015-09-26)
The bioorthogonal keto group has attracted interest for the site-specific chemical conjugation of recombinant proteins under mild conditions, e.g. with aminooxy-functionalised fluorescent probes, radiometal chelates, toxins or polymers. However, the cotranslational incorporation of the corresponding non-canonical amino acid p-acetyl-L-phenylalanine (Apa)
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