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A16300

Sigma-Aldrich

N-Acetylglycine

ReagentPlus®, 99%

Sinónimos:

Acetamidoacetic acid, Aceturic acid

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About This Item

Fórmula lineal:
CH3CONHCH2CO2H
Número de CAS:
543-24-8
Peso molecular:
117.10
Beilstein/REAXYS Number:
774114
EC Number:
208-839-6
MDL number:
MFCD00004275
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24890569
NACRES:
NA.22

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

SMILES string

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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Legal Information

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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
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
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)
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
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