330469
N-Phenylglycine
97%
Synonym(s):
(Phenylamino)acetic acid, Anilinoacetic acid
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About This Item
Linear Formula:
C6H5NHCH2COOH
CAS Number:
Molecular Weight:
151.16
Beilstein:
509838
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
reaction suitability
reaction type: solution phase peptide synthesis
mp
121-123 °C (lit.)
application(s)
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)
InChI key
NPKSPKHJBVJUKB-UHFFFAOYSA-N
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Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A D Johnston et al.
Journal of dental research, 68(9), 1337-1344 (1989-09-01)
Using bond strength measurements, we investigated a number of related compounds in order to elucidate the role of the surface-active ingredient, N-phenylglycine (NPG), in experimental two-step and three-step bonding protocols resulting in adhesive bonding to dentin. All active compounds identified
Y Imai et al.
Dental materials : official publication of the Academy of Dental Materials, 10(4), 275-277 (1994-07-01)
This research was designed to study the effect of water or carboxylic acid monomer on the polymerization of 2-hydroxyethyl methacrylate (HEMA) in order to understand the bonding mechanism of dentin bonding systems using N-phenylglycine (NPG). The polymerization of HEMA in
P E Reifeis et al.
Operative dentistry, 20(5), 174-179 (1995-09-01)
The purpose of this study was to compare the enamel shear bond strengths achieved with four acid conditioners employed by current enamel/dentin bonding systems (maleic acid, citric acid, nitric acid, oxalic acid) with a 37% phosphoric acid etching technique. The
Design and synthesis of photochemically controllable caspase-3.
Masayuki Endo et al.
Angewandte Chemie (International ed. in English), 43(42), 5643-5645 (2004-10-21)
Mohamed A Elsawy et al.
Journal of peptide science : an official publication of the European Peptide Society, 18(5), 302-311 (2012-03-28)
We have been engaged in the microwave-solid phase peptide synthesis (SPPS) synthesis of the phenylglycine (Phg)-containing pentapeptide H-Ala-Val-Pro-Phg-Tyr-NH(2) (1) previously demonstrated to bind to the so-called BIR3 domain of the anti-apoptotic protein XIAP. Analysis of the target peptide by a
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