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Merck
CN

215333

4-Hydroxy-D-phenylglycine

≥98%

Synonym(s):

(2R)-2-Amino-2-(4-hydroxyphenyl)acetic acid

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About This Item

Linear Formula:
HOC6H4CH(NH2)CO2H
CAS Number:
22818-40-2
Molecular Weight:
167.16
NACRES:
NA.22
PubChem Substance ID:
24852886
eCl@ss:
32160406
UNSPSC Code:
41116107
EC Number:
245-247-7
MDL number:
MFCD00004262
Beilstein/REAXYS Number:
2210998

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Product Name

4-Hydroxy-D-phenylglycine, ≥98%

InChI key

LJCWONGJFPCTTL-SSDOTTSWSA-N

InChI

1S/C8H9NO3/c9-7(8(11)12)5-1-3-6(10)4-2-5/h1-4,7,10H,9H2,(H,11,12)/t7-/m1/s1

SMILES string

N[C@@H](C(O)=O)c1ccc(O)cc1

assay

≥98%

form

solid

optical activity

[α]23/D −158±3°, c = 1 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

240 °C (dec.) (lit.)

application(s)

peptide synthesis

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Storage Class

13 - Non 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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Certificates of Analysis (COA)

Lot/Batch Number
WXBD9053V
MKCM1690
MKCG9060
MKCB4680
MKBV6483V

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Tony Ly et al.
Journal of the American Society for Mass Spectrometry, 20(6), 1148-1158 (2009-03-17)
Photodissociation of iodo-tyrosine modified peptides yields localized radicals on the tyrosine side chain, which can be further dissociated by collisional activation. We have performed extensive experiments on model peptides, RGYALG, RGYG, and their derivatives, to elucidate the mechanisms underlying backbone
Mònica Prieto et al.
The Journal of organic chemistry, 74(23), 9202-9205 (2009-10-30)
Alpha-amino acid derivatives, particularly those of phenylglycine, can suffer significant racemization in Suzuki couplings. When arylpinacolboronate esters are used as coupling partners this unwanted side reaction can be suppressed by the use of Pd(OAc)(2) as Pd(0) source, in the presence
Stephan Kastner et al.
Archives of microbiology, 194(6), 557-566 (2012-02-07)
The nonproteinogenic amino acid 4-hydroxyphenylglycine (HPG) arises from the diversion of the tyrosine degradation pathway into secondary metabolism, and its biosynthesis requires a set of three enzymes. The gene cassette for HPG biosynthesis is widely spread in actinomycete bacteria, which
Jeanne M Davidsen et al.
Journal of bacteriology, 191(3), 1066-1077 (2008-11-26)
Nocardicin A is a monocyclic beta-lactam isolated from the actinomycete Nocardia uniformis, which shows moderate activity against a broad spectrum of gram-negative bacteria. Within the biosynthetic gene cluster of nocardicin A, nocR encodes a 583-amino-acid protein with high similarity to
Naotoshi Hirota et al.
Life sciences, 79(13), 1312-1316 (2006-05-19)
To assess the mechanism of beta-cell lipotoxicity in comparison with Fas-mediated cell death, we used a mouse beta-cell clone stably transfected with human Fas. Palmitate induced beta-cell death in correlation with medium glucose levels between 5 and 20 mmol/l, while
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