Chemical Properties of N-«alpha»-Acetylglycinamide (CAS 2620-63-5)

N-«alpha»-Acetylglycinamide

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InChI
InChI=1S/C4H8N2O2/c1-3(7)6-2-4(5)8/h2H2,1H3,(H2,5,8)(H,6,7)
InChI Key
WQELDIQOHGAHEM-UHFFFAOYSA-N
Formula
C4H6N2O2
SMILES
CC(=O)NCC(N)=O
Molecular Weight1
114.10
CAS
2620-63-5
Other Names
  • N-Acetylglycine amide
  • Acetamide, N-(2-amino-2-oxoethyl)-
  • N-Acetylglycinamide
  • 2-acetamidoacetamide
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Physical Properties

Property Value Unit Source
Δf -119.20 kJ/mol Joback Calculated Property
Δfgas -263.79 kJ/mol Joback Calculated Property
Δfus 19.61 kJ/mol Joback Calculated Property
Δsub [140.20; 140.20] kJ/mol Show Hide
Δsub 140.20 ± 2.30 kJ/mol NIST
Δsub 140.20 ± 2.30 kJ/mol NIST
Δvap 55.07 kJ/mol Joback Calculated Property
log10WS 0.33 Crippen Calculated Property
logPoct/wat -1.392 Crippen Calculated Property
McVol 90.320 ml/mol McGowan Calculated Property
Pc 5058.59 kPa Joback Calculated Property
Tboil 521.36 K Joback Calculated Property
Tc 729.58 K Joback Calculated Property
Tfus 370.62 K Joback Calculated Property
Vc 0.336 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [200.29; 242.42] J/mol×K [521.36; 729.58] Show Hide
Cp,gas 200.29 J/mol×K 521.36 Joback Calculated Property
Cp,gas 208.37 J/mol×K 556.06 Joback Calculated Property
Cp,gas 216.02 J/mol×K 590.77 Joback Calculated Property
Cp,gas 223.24 J/mol×K 625.47 Joback Calculated Property
Cp,gas 230.04 J/mol×K 660.18 Joback Calculated Property
Cp,gas 236.43 J/mol×K 694.88 Joback Calculated Property
Cp,gas 242.42 J/mol×K 729.58 Joback Calculated Property
ΔfusH [25.60; 25.60] kJ/mol [408.20; 408.20] Show Hide
ΔfusH 25.60 kJ/mol 408.20 NIST
ΔfusH 25.60 kJ/mol 408.20 NIST
ΔfusH 25.60 kJ/mol 408.20 NIST
ΔfusH 25.60 kJ/mol 408.20 NIST
ΔsubH [123.50; 135.00] kJ/mol [376.00; 392.00] Show Hide
ΔsubH 123.50 ± 1.70 kJ/mol 376.00 NIST
ΔsubH 135.00 ± 3.00 kJ/mol 392.00 NIST
ΔfusS 62.70 J/mol×K 408.20 NIST

Similar Compounds

2-(Acetylamino)-N-methylethanamide. 2,5-Piperazinedione. N-Acetylethylenediamine. Glycylglycylglycylglycine. Hexaglycine. N-Glycylglycine. N-[N-(Trifluoroacetyl)glycylglycine. N-(2-aminoethyl) mercaptoacetamide. N-Acetyl-L-alanine amide. Glycine, N-acetyl-. Acetamide, N-ethyl-. N,n'-ethylenebis(mercaptoacetamide). Glycine, N-[N-(trifluoroacetyl)glycyl]-, methyl ester. gly-gly-ala. N,N'-Diethyloxamide.

Find more compounds similar to N-«alpha»-Acetylglycinamide.

Sources

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