ChemicalBook--->CAS DataBase List--->15873-51-5

15873-51-5

15873-51-5 Structure

15873-51-5 Structure
IdentificationBack Directory
[Name]

4-NITROANILINE HYDROCHLORIDE
[CAS]

15873-51-5
[Synonyms]

Einecs 239-997-4
4-nitroanilinium chloride
1-Amino-4-nitrobenzeneHCl
P-NITRANILINE HYDROCHLORIDE
P-NITROANILINE HYDROCHLORIDE
4-NITROANILINE HYDROCHLORIDE
4-NITROPHENYLAMINE HYDROCHLORIDE
4-nitro-benzenaminmonohydrochloride
1-AMINO-4-NITROBENZENE HYDROCHLORIDE
Benzenamine, 4-nitro-, monohydrochloride
Benzenamine, 4-nitro-, hydrochloride (1:1)
[EINECS(EC#)]

239-997-4
[Molecular Formula]

C6H7ClN2O2
[MDL Number]

MFCD00054338
[MOL File]

15873-51-5.mol
[Molecular Weight]

174.58
Chemical PropertiesBack Directory
[Melting point ]

145-146 °C
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[color ]

Light yellow to Amber to Dark green
[EPA Substance Registry System]

Benzenamine, 4-nitro-, monohydrochloride (15873-51-5)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H336-H361-H370-H372-H412
[Precautionary statements ]

P201-P202-P260-P264-P270-P271-P273-P280-P301+P312+P330-P304+P340+P312-P307+P311-P403+P233-P405-P501
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[TSCA ]

TSCA listed
[HS Code ]

2921.42.9000
Spectrum DetailBack Directory
[Spectrum Detail]

4-NITROANILINE HYDROCHLORIDE(15873-51-5)1HNMR
4-NITROANILINE HYDROCHLORIDE(15873-51-5)IR1
4-NITROANILINE HYDROCHLORIDE(15873-51-5)IR2
Hazard InformationBack Directory
[Synthesis]

1,4-DINITROBENZENE

100-25-4

4-NITROANILINE HYDROCHLORIDE

15873-51-5

GENERAL METHOD: To a 0.6 mL THF solution of the nitro compound (2 mmol) was added Fe(acac)3 (10 mol%, 70 mg) and TMDS (1.5 eq., equivalent to tris-Si-H, 0.53 mL). The reaction mixture was heated under constant stirring for 24 hours (unless otherwise stated). Upon completion of the reaction, the reaction mixture was diluted with a minimal amount of Et2O. Subsequently, a solution of Et2O with HCl (2 equivalents) was added dropwise. After precipitate generation was observed, stirring was continued for 5 minutes and then filtered. The precipitate was washed several times with Et2O and dried to give 4-nitroaniline hydrochloride.

[References]

[1] Tetrahedron, 2011, vol. 67, # 10, p. 1971 - 1976
[2] Journal of Organic Chemistry, 2009, vol. 74, # 18, p. 6960 - 6964
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