280216
Nα-Acetylglycinamide
97%
Synonym(s):
2-Acetamidoacetamide
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About This Item
Linear Formula:
CH3CONHCH2CONH2
CAS Number:
Molecular Weight:
116.12
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
140-143 °C (lit.)
SMILES string
CC(=O)NCC(N)=O
InChI
1S/C4H8N2O2/c1-3(7)6-2-4(5)8/h2H2,1H3,(H2,5,8)(H,6,7)
InChI key
WQELDIQOHGAHEM-UHFFFAOYSA-N
Application
Nα-Acetylglycinamide (2-Acetamidoacetamide) was used in the preparation of 3-unsubstituted 2-pyridones by a tandem reaction with chalcones[1].
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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[The systems analysis of the effect of piracetam, glycine and N-acetylglycinamide on long-term learning].
A I Machula et al.
Eksperimental'naia i klinicheskaia farmakologiia, 56(4), 55-57 (1993-07-01)
V I Naumova et al.
Biulleten' eksperimental'noi biologii i meditsiny, 107(6), 711-713 (1989-06-01)
The effect of electroshock (ECS) and piracetam, oxiracetam or N-acetylglycinamide on the passive avoidance conditioned response in rats was studied. The antiemetic effect of the compounds was examined in cats as well. The results obtained allowed us to distinct the
Tomohisa Nezu et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 32(5), 844-850 (2012-01-19)
Limited evidence exists on the relationships between severity of white-matter lesions (WMLs) and cerebral hemodynamics in patients without major cerebral artery disease. To examine changes of cerebral blood flow (CBF), oxygen metabolism, and vascular reserve capacity associated with severity of
Matthew Auton et al.
Biochemistry, 43(5), 1329-1342 (2004-02-06)
With knowledge of individual transfer free energies of chemical groups that become newly exposed on protein denaturation and assuming the group transfer free energy contributions are additive, it should be possible to predict the stability of a protein in the
Gregory A Chass et al.
The journal of physical chemistry. A, 109(24), 5289-5302 (2006-07-15)
Computational and experimental determinations were carried out in parallel on the conformational probability of N-Acetyl-Phenylalanine-NH2 (NAPA). Ab initio computations were completed at the BLYP/6-311G(df,p), B3LYP/6-31G(d), B3LYP/6-31G(d,p), and B3LYP/6-31+G(d) levels of theory, labeled L/61fp, B/6, B/6p, and B/6+, respectively. Three experimentally
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