Merck
CN
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文件

A16300

Sigma-Aldrich

N-乙酰甘氨酸

ReagentPlus®, 99%

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别名:
乙酰氨基乙酸, 醋尿酸
线性分子式:
CH3CONHCH2CO2H
CAS号:
543-24-8
分子量:
117.10
Beilstein:
774114
EC 号:
208-839-6
MDL编号:
MFCD00004275
eCl@ss:
32160406
PubChem化学物质编号:
24890569
NACRES:
NA.22

质量水平

200

产品线

ReagentPlus®

检测方案

99%

形式

powder or crystals

反应适用性

reaction type: C-H Activation
reaction type: solution phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

颜色

white

mp

207-209 °C (lit.)

应用

detection
peptide synthesis

官能团

amine
carboxylic acid

SMILES字符串

CC(=O)NCC(O)=O

InChI

1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8)

InChI key

OKJIRPAQVSHGFK-UHFFFAOYSA-N

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相关类别

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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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
Liangxing Wu et al.
Journal of the American Chemical Society, 130(12), 4089-4096 (2008-03-07)
Eight B-containing compounds, i.e., 1a-h, were prepared as mimics of the green fluorescent protein (GFP) fluorophore. The underlying concept was that synthetic GFP chromophore analogues are not fluorescent primarily because of free rotation about an aryl-alkene bond (Figure 1b). This
H K Ogawa et al.
Journal of chromatography, 612(1), 145-149 (1993-01-29)
A simple and sensitive method for the determination of N-acetylneuraminic acid and N-glycolylneuraminic acid in glycoproteins by high-performance liquid chromatography has been investigated. The best condition to release sialic acid from glycoproteins involved incubation at 80 degrees C for 1
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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