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Sigma-Aldrich

Nα-Acetylglycinamide

97%

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Synonym(s):
2-Acetamidoacetamide
Linear Formula:
CH3CONHCH2CONH2
CAS Number:
2620-63-5
Molecular Weight:
116.12
EC Number:
220-058-2
MDL number:
MFCD00008029
PubChem Substance ID:
24856939
NACRES:
NA.22

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

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

Regulatory Information

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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
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
A Regioselective Tandem Reaction between Chalcones and 2-Acetamidoacetamide Promoted by Cs2 CO3 for the Preparation of 3-Unsubstituted 2-Pyridones.
Wang S, et al.
Synthesis, 2003(04), 0487-0490 (2003)
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