Chemical Properties of chlornaphazine (CAS 494-03-1)

chlornaphazine

InChI
InChI=1S/C14H15Cl2N/c15-7-9-17(10-8-16)14-6-5-12-3-1-2-4-13(12)11-14/h1-6,11H,7-10H2
InChI Key
XCDXSSFOJZZGQC-UHFFFAOYSA-N
Formula
C14H15Cl2N
SMILES
ClCCN(CCCl)c1ccc2ccccc2c1
Molecular Weight1
268.18
CAS
494-03-1
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Physical Properties

Property Value Unit Source
ω 0.6410 Relay (1.0) Calculated Property
ΔfG° 363.35 kJ/mol Joback Calculated Property
ΔfH°gas 72.96 kJ/mol Relay (1.0) Calculated Property
ΔfusH° 34.10 kJ/mol Joback Calculated Property
ΔvapH° 90.40 kJ/mol Relay (1.0) Calculated Property
IE 7.57 eV Relay (1.0) Calculated Property
log10WS -5.38 Relay (1.0) Calculated Property
logPoct/wat 4.124 Crippen Calculated Property
McVol 199.360 ml/mol McGowan Calculated Property
Pc 2318.07 kPa Joback Calculated Property
Tboil 648.49 K Relay (1.0) Calculated Property
Tc 901.06 K Relay (1.0) Calculated Property
Tfus 328.00 ± 1.00 K NIST
Vc 0.689 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [482.48; 555.81] J/mol×K [657.66; 883.23] Show Hide
Cp,gas 482.48 J/mol×K 657.66 Joback Calculated Property
Cp,gas 497.09 J/mol×K 695.26 Joback Calculated Property
Cp,gas 510.62 J/mol×K 732.85 Joback Calculated Property
Cp,gas 523.16 J/mol×K 770.45 Joback Calculated Property
Cp,gas 534.81 J/mol×K 808.04 Joback Calculated Property
Cp,gas 545.67 J/mol×K 845.64 Joback Calculated Property
Cp,gas 555.81 J/mol×K 883.23 Joback Calculated Property

Pressure Dependent Properties

Property Value Unit Pressure (kPa) Source
Tboilr [483.00; 483.20] K [0.70; 0.70] Show Hide
Tboilr 483.20 K 0.70 NIST
Tboilr 483.00 K 0.70 NIST

Similar Compounds

Aniline mustard. Diethyl-«alpha»-naphthylamine. N,N-Bis(2-hydroxyethyl)-2-naphthylamine. p-N,N-Bis(2-chloroethyl)aminobenzoic acid. 4-Bis(2-chloroethyl)aminobenzaldehyde. p-([2-Chloroethyl]ethylamino)benzaldehyde. Alpha-chloro-n-ethyl acetanilide. N,N-Diethylaniline. 4-N,N-Bis(2-chloroethyl)amino-2-tolualdehyde. N,N-Diethyl-3-nitroaniline. Ethanol, 2,2'-(phenylimino)bis-. 3,3'-(Phenylimino)dipropionitrile. Ethanol, 2-(ethylphenylamino)-. Phenol, 3-(diethylamino)-. Propanenitrile, 3-(ethylphenylamino)-.

Find more compounds similar to chlornaphazine.

Sources

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