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
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
Quality Level
application(s)
detection
peptide synthesis
functional group
amine, carboxylic acid
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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)
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
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
Jamie L Snow et al.
Journal of the American Chemical Society, 129(32), 9910-9917 (2007-07-26)
Both theoretical and experimental studies are reported for the gas-phase reactions of protonated hydroxylamine with acetic and propanoic acids which yield protonated glycine and alanine, GlyH+ and AlaH+, respectively. The key step for these reactions is an insertion of the
S K Mehta et al.
Journal of colloid and interface science, 314(2), 689-698 (2007-06-26)
The well-characterized, monodisperse nature of reverse micelles formed by sodium bis-(2-ethylhexyl)sulfosuccinate/water/isooctane and their usefulness in assimilating compounds of varied interests have been exploited to investigate the effect of acetyl modified amino acids (MAA) viz., N-acetyl-L-glycine (NAG), N-acetyl-L-aspartic acid (NAA) and
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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