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Dokumente

330469

Sigma-Aldrich

N-Phenylglycin

97%

Synonym(e):

Anilinoessigsäure, Phenylaminoessigsäure

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About This Item

Lineare Formel:
C6H5NHCH2COOH
CAS-Nummer:
103-01-5
Molekulargewicht:
151.16
Beilstein:
509838
EG-Nummer:
203-070-2
MDL-Nummer:
MFCD00014009
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24859860
NACRES:
NA.22

Qualitätsniveau

200

Assay

97%

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

121-123 °C (lit.)

Anwendung(en)

peptide synthesis

SMILES String

OC(=O)CNc1ccccc1

InChI

1S/C8H9NO2/c10-8(11)6-9-7-4-2-1-3-5-7/h1-5,9H,6H2,(H,10,11)

InChIKey

NPKSPKHJBVJUKB-UHFFFAOYSA-N

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Borandimethylamin-Komplex 97%

Sigma-Aldrich

180238

Borandimethylamin-Komplex

N-Methyldiethanolamin ≥99%

Sigma-Aldrich

471828

N-Methyldiethanolamin

J M Janusz et al.
Journal of medicinal chemistry, 33(3), 1052-1061 (1990-03-01)
Twenty esters of L-aspartyl-D-phenylglycine, as well as two substituted analogues, an o-fluoro and a p-hydroxy-phenylglycine ester, were prepared. The L-aspartyl-D-phenylglycine (-)-alpha- and (+)-beta-fenchyl esters had the highest sweetness potency at 1200 and 3700 times that of sucrose, respectively. The high
G E Schumacher et al.
Journal of dental research, 76(1), 602-609 (1997-01-01)
Effective composite-to-dentin bonding has been achieved by the sequential use of dilute aqueous nitric acid (HNO3) and acetone solutions of N-phenylglycine and a carboxylic acid monomer, e.g., p-PMDM. Both the HNO3 pre-treatment and the surface-initiated polymerization that results from reaction
L E Wolinsky et al.
Journal of dental research, 72(1), 72-77 (1993-01-01)
The purpose of the present investigation was to determine whether high-resolution carbon-13 nuclear magnetic resonance could be utilized for detection of ionic bonding interactions of NPG and NPG-GMA with selected inorganic cations. The C1-carbonyl carbon of NPG and NPG-GMA were
N J Miniotis et al.
Journal of dental research, 72(6), 1045-1049 (1993-06-01)
This study evaluated and compared the contributions to dentin adhesive bonding of three N-phenylglycine analogues with electron-withdrawing substituents on the aromatic ring. These electron-deficient "N-compounds" included: N-(4-chlorophenyl)-glycine (NCPG), N-methyl-N-(4-chlorophenyl)-glycine (NMNCPG), and N-(3,4-dichlorophenyl)-glycine (NDCPG). An experimental three-step dentin-bonding protocol that consisted
G Kato et al.
Dental materials : official publication of the Academy of Dental Materials, 14(5), 347-352 (1999-06-24)
The purpose of this study was to investigate the influence of remaining non-resin-impregnated, phosphoric acid demineralized dentin upon the long-term durability of specimens that were wet-bonded to bovine dentin substrates. Prepared bovine dentin samples were etched with 65% phosphoric acid
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