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Merck

147966

DL-Phenylalanine

99%, for peptide synthesis, ReagentPlus®

Sinónimos:

(±)-2-Amino-3-phenylpropionic acid

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Acerca de este artículo

Fórmula lineal:
C6H5CH2CH(NH2)COOH
Número CAS:
Peso molecular:
165.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
205-756-7
MDL number:
Beilstein/REAXYS Number:
3198807
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Nombre del producto

DL-Phenylalanine, ReagentPlus®, 99%

InChI key

COLNVLDHVKWLRT-UHFFFAOYSA-N

InChI

1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)

SMILES string

NC(Cc1ccccc1)C(O)=O

product line

ReagentPlus®

assay

99%

form

powder, crystals or granules

reaction suitability

reaction type: solution phase peptide synthesis

mp

266-267 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

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Application

DL-Phenylalanine may be used in the synthesis of ternary piroxicam (Pir; 4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II).

General description

Phenylalanine is an amino acid. It participates in the preparation of ternary piroxicam complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II). Characterization of these complexes by elemental analyses, molar conductance, IR, UV-Vis, magnetic moment, diffuse reflectance and X-ray powder diffraction methods has been conducted. Crystalline DL-phenylalanine was prepared by its reduction in silica gel by solubility method.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Gehad G Mohamed et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(13), 3141-3154 (2004-10-13)
The ternary piroxicam (Pir; 4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) with various amino acids (AA) such as glycine (Gly) or DL-phenylalanine (PhA) were prepared and characterized by elemental analyses, molar conductance, IR, UV-Vis, magnetic moment
XRD, thermal and FTIR studies on gel grown DL-Phenylalanine crystals.
Ramachandran E and Natarajan S.
Crystal Research and Technology, 42(6), 617-620 (2007)
Raja R Pillai et al.
The Journal of nutrition, 145(5), 954-959 (2015-03-13)
Lysine requirements of well-nourished children from developing regions have been found to be similar to those of children from developed regions (33.5 mg · kg⁻¹ · d⁻¹). However, intestinal parasites have been shown to increase lysine requirements in undernourished adults, and it is not
Katarzyna M Romek et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(27), 8296-8301 (2015-06-25)
Tramadol, previously only known as a synthetic analgesic, has now been found in the bark and wood of roots of the African medicinal tree Nauclea latifolia. At present, no direct evidence is available as to the biosynthetic pathway of its
Sohei Nakayama et al.
Cancer research, 74(20), 5891-5902 (2014-08-29)
The discovery of somatic mutations in EGFR and development of EGFR tyrosine kinase inhibitors (TKI) have revolutionized treatment for lung cancer. However, resistance to TKIs emerges in almost all patients and currently no effective treatment is available. Here, we show

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