Chemical Properties of 4-Dimethylamino-o-tolualdehyde (CAS 1199-59-3)

4-Dimethylamino-o-tolualdehyde

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InChI
InChI=1S/C10H13NO/c1-8-6-10(11(2)3)5-4-9(8)7-12/h4-7H,1-3H3
InChI Key
XZWMCPUAUNHGPF-UHFFFAOYSA-N
Formula
C10H13NO
SMILES
Cc1cc(N(C)C)ccc1C=O
Molecular Weight1
163.22
CAS
1199-59-3
Other Names
  • Benzaldehyde, 4-(dimethylamino)-2-methyl-
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Physical Properties

Property Value Unit Source
Δf 137.73 kJ/mol Joback Calculated Property
Δfgas -54.19 kJ/mol Joback Calculated Property
Δfus 20.23 kJ/mol Joback Calculated Property
Δvap 50.22 kJ/mol Joback Calculated Property
log10WS -2.10 Crippen Calculated Property
logPoct/wat 1.874 Crippen Calculated Property
McVol 139.550 ml/mol McGowan Calculated Property
Pc 3069.34 kPa Joback Calculated Property
Tboil 525.94 K Joback Calculated Property
Tc 734.81 K Joback Calculated Property
Tfus 328.39 K Joback Calculated Property
Vc 0.522 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [311.18; 381.78] J/mol×K [525.94; 734.81] Show Hide
Cp,gas 311.18 J/mol×K 525.94 Joback Calculated Property
Cp,gas 324.80 J/mol×K 560.75 Joback Calculated Property
Cp,gas 337.64 J/mol×K 595.56 Joback Calculated Property
Cp,gas 349.73 J/mol×K 630.38 Joback Calculated Property
Cp,gas 361.10 J/mol×K 665.19 Joback Calculated Property
Cp,gas 371.77 J/mol×K 700.00 Joback Calculated Property
Cp,gas 381.78 J/mol×K 734.81 Joback Calculated Property

Similar Compounds

N,N-Dimethyl-3,4-xylidine. 4-N,N-Bis(2-chloroethyl)amino-2-tolualdehyde. N-Methyl-3,4-xylidine. Benzenamine, N,N,3-trimethyl-. Benzenamine, N,N-diethyl-3-methyl-. Benzaldehyde, 4-(dimethylamino)-. Trifluoroacetamide, N-methyl-N-(3-methylphenyl)-. 3',4'-Acetoxylide. N,N,2,4-Tetramethylbenzenamine. N-(m-Tolyl)-diethanolamine. 2-(N-Ethyl-N-toluidino)ethanol, methyl ether. Ethanol, 2-[ethyl(3-methylphenyl)amino]-. Benzaldehyde, 4-(diethylamino)-. 2-(N-Ethyl-N-tolylamino)ethanol, trifluoroacetate. Benzaldehyde, 2-chloro-4-dimethylamino-.

Find more compounds similar to 4-Dimethylamino-o-tolualdehyde.

Sources

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