330469
N-苯基甘氨酸
97%
别名:
苯胺乙酸, 苯胺基醋酸
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线性分子式:
C6H5NHCH2COOH
化学文摘社编号:
分子量:
151.16
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-070-2
Beilstein/REAXYS Number:
509838
MDL number:
产品名称
N-苯基甘氨酸, 97%
assay
97%
SMILES string
OC(=O)CNc1ccccc1
InChI key
NPKSPKHJBVJUKB-UHFFFAOYSA-N
InChI
1S/C8H9NO2/c10-8(11)6-9-7-4-2-1-3-5-7/h1-5,9H,6H2,(H,10,11)
reaction suitability
reaction type: solution phase peptide synthesis
mp
121-123 °C (lit.)
application(s)
peptide synthesis
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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
Zhongqiao Hu et al.
The journal of physical chemistry. B, 113(48), 15851-15857 (2009-11-10)
A microscopic understanding of chiral separation mechanisms in liquid chromatography is significant in the pharmaceutical industry to facilitate the rational design of novel stationary phases and the optimization of separation processes. A molecular simulation study is reported to investigate the
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
J Watkins et al.
Trends in pharmacological sciences, 15(9), 333-342 (1994-09-01)
Metabotropic glutamate receptors represent a family of G protein-coupled receptors that can be activated by L-glutamate, the principal excitatory neurotransmitter in the brain. Until recently, progress in identifying the physiological and pathological roles of metabotropic glutamate receptors has been hampered
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