A16300
N-乙酰甘氨酸
ReagentPlus®, 99%
别名:
乙酰氨基乙酸, 醋尿酸
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关于此项目
线性分子式:
CH3CONHCH2CO2H
化学文摘社编号:
分子量:
117.10
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
208-839-6
MDL number:
Beilstein/REAXYS Number:
774114
产品名称
N-乙酰甘氨酸, ReagentPlus®, 99%
InChI key
OKJIRPAQVSHGFK-UHFFFAOYSA-N
InChI
1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8)
SMILES string
CC(=O)NCC(O)=O
product line
ReagentPlus®
assay
99%
form
powder or crystals
reaction suitability
reaction type: C-H Activation
reaction type: solution phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis
color
white
mp
207-209 °C (lit.)
application(s)
detection
peptide synthesis
functional group
amine
carboxylic acid
Quality Level
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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)
Z Gu et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 138(2), 193-198 (1999-05-26)
Triple-resonance experiments capable of correlating directly bonded and proximate carbon and nitrogen backbone sites of uniformly 13C- and 15N-labeled peptides in stationary oriented samples are described. The pulse sequences integrate cross-polarization from 1H to 13C and from 13C to 15N
Y Chen et al.
Biochemistry, 37(28), 9976-9982 (1998-07-17)
A general approach to dissecting the complex photophysics of tryptophan is presented and used to elucidate the effects of amino acid functional groups on tryptophan fluorescence. We have definitively identified the amino acid side chains that quench tryptophan fluorescence and
Anatoliy Volkov et al.
Journal of computational chemistry, 25(7), 921-934 (2004-03-18)
Accurate and fast evaluation of electrostatic interactions in molecular systems is still one of the most challenging tasks in the rapidly advancing field of macromolecular chemistry, including molecular recognition, protein modeling and drug design. One of the most convenient and
Bram Boeckx et al.
The journal of physical chemistry. A, 116(8), 1956-1965 (2012-01-26)
Within the structure determination task for peptides, which is of large interest due to the relation between structure and functionality, infrared spectra can provide detailed information on the conformational behavior. The conformational landscape ofN-acetylgycine has been studied by a combined
Functionalizing glycine derivatives by direct C-C bond formation.
Liang Zhao et al.
Angewandte Chemie (International ed. in English), 47(37), 7075-7078 (2008-08-02)
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