Chemical Properties of Benzenamine, 4-methoxy-2-nitro- (CAS 96-96-8)

InChI

InChI=1S/C7H8N2O3/c1-12-5-2-3-6(8)7(4-5)9(10)11/h2-4H,8H2,1H3

InChI Key

QFMJFXFXQAFGBO-UHFFFAOYSA-N

Formula

C7H8N2O3

SMILES

COc1ccc(N)c([N+](=O)[O-])c1

Molecular Weight¹

168.15

CAS

96-96-8

Other Names

• p-Anisidine, 2-nitro-
• Acco Fast Bordeaux GP Salt
• Amarthol Fast Bordeaux GP Base
• Amarthol Fast Bordeaux GP Salt
• Atul Fast Bordeaux GP Base
• Azobase NAS
• Azoene Fast Bordeaux GP Base
• Azoene Fast Bordeaux GP Salt
• Azofix Bordeaux GP
• Azogene Fast Bordeaux G
• Bordeaux Base Ciba IV
• Bordeaux Base Irga IV
• Bordeaux Base NGP
• Bordeaux GP Base
• Bordeaux GP Salt
• Bordeaux GPS Salt
• Bordeaux Salt Ciba IV
• Bordeaux Salt NGP
• Brentamine Fast Bordeaux GP Base
• C.I. Azoic Diazo Component 1
• C.I. 37135
• Daito Bordeaux Base GP
• Daito Bordeaux Salt GP
• Devol Bordeaux B
• Devol Bordeaux GP Salt
• Diabase Bordeaux GP
• Diasalt Bordeaux GP
• Diazo Fast Bordeaux GP
• Durgasol Bordeaux GP Salt
• Fast Bordeaux Base GP
• Fast Bordeaux Base J
• Fast Bordeaux GDN
• Fast Bordeaux GP
• Fast Bordeaux GP Base
• Fast Bordeaux GP Salt
• Fast Bordeaux GPN Base
• Fast Bordeaux Salt GP
• Fast Bordeaux Salt GPN
• Fast Bordeaux Salt J
• Fast Bordeaux 3NA Base
• Hansol Bordeaux GP Salt
• Hiltonil Fast Bordeaux GP Base
• Hiltosal Fast Bordeaux GP Salt
• Hindasol Bordeaux GP Salt
• Kako Bordeaux GP Base
• Kako Bordeaux GP Salt
• Kayaku Fast Bordeaux GP Base
• Kayaku Fast Bordeaux Salt GP
• Lake Maroon B Base
• Mitsui Bordeaux GP Base
• Mitsui Bordeaux GP Salt
• Naphthanil Bordeaux GP Base
• Naphthanil Diazo Bordeaux GP
• Naphthosol Fast Bordeaux GP Salt
• Naphtoelan Fast Bordeaux GP Base
• Naphtoelan Fast Bordeaux GP Salt
• Natasol Bordeaux GP Salt
• Pharmasol Bordeaux GP
• Pharmazoid Bordeaux GP
• Sanyo Fast Bordeaux GP Base
• Sanyo Fast Bordeaux Salt GP
• Shinnippon Fast Bordeaux GP Base
• Sugai Fast Bordeaux GP Base
• Symulon Bordeaux GP Base
• Tulabase Fast Bordeaux GP
• 2-Nitro-p-anisidine
• 2-Nitro-4-methoxyaniline
• 3-Nitro-4-aminoanisole
• 4-Amino-3-nitroanisole
• 4-Methoxy-2-nitroaniline
• Aniline, 4-methoxy-2-nitro-
• Gp-amin
• o-Nitro-p-anisidine
• 4-Methoxy-o-nitroaniline
• 4-Methoxy-2-nitrophenylamine
• 1-Amino-2-nitro-4-methoxybenzene
• Fast Bordeaux GDN base
• 2-Nitro-4-methoxybenzenamine
• 4-Methoxy-2-nitrohbenzenamine

• C_p,gas : Ideal gas heat capacity (J/mol×K).
• Δ_fG° : Standard Gibbs free energy of formation (kJ/mol).
• Δ_fH°_gas : Enthalpy of formation at standard conditions (kJ/mol).
• Δ_fusH° : Enthalpy of fusion at standard conditions (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• log₁₀WS : Log10 of Water solubility in mol/l.
• logP_oct/wat : Octanol/Water partition coefficient.
• McVol : McGowan's characteristic volume (ml/mol).
• P_c : Critical Pressure (kPa).
• T_boil : Normal Boiling Point Temperature (K).
• T_c : Critical Temperature (K).
• T_fus : Normal melting (fusion) point (K).
• V_c : Critical Volume (m³/kmol).
• ¹: Molecular weight from the IUPAC atomic weights tables.

Physical Properties

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[291.35; 343.08]	J/mol×K	[642.99; 896.92]
Cp,gas	291.35	J/mol×K	642.99	Joback Calculated Property
Cp,gas	301.87	J/mol×K	685.31	Joback Calculated Property
Cp,gas	311.62	J/mol×K	727.63	Joback Calculated Property
Cp,gas	320.60	J/mol×K	769.95	Joback Calculated Property
Cp,gas	328.83	J/mol×K	812.28	Joback Calculated Property
Cp,gas	336.32	J/mol×K	854.60	Joback Calculated Property
Cp,gas	343.08	J/mol×K	896.92	Joback Calculated Property

Similar Compounds

Find more compounds similar to Benzenamine, 4-methoxy-2-nitro-.

Sources

• Crippen Method
• Crippen Method
• Joback Method
• McGowan Method
• NIST Webbook

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