ChemicalBook--->CAS DataBase List--->1775-95-7

1775-95-7

1775-95-7 Structure

1775-95-7 Structure
IdentificationMore
[Name]

2-Amino-5-nitrobenzophenone
[CAS]

1775-95-7
[Synonyms]

2-AMINO-5-NITROBENZOPHENONE
(2-AMINO-5-NITRO-PHENYL)-PHENYL-METHANONE
IFLAB-BB F0266-0701
LABOTEST-BB LT00000253
TIMTEC-BB SBB000821
(2-amino-5-nitrophenyl)phenyl-methanon
2-Amino-5-nitrodiphenylmethone
2-Amino-5-nitrodiphenylone
2-Benzoyl-4-nitroaniline
5-Nitro-2-aminobenzophenone
Benzophenone, 2-amino-5-nitro-
Methanone, (2-amino-5-nitrophenyl)phenyl-
Methanone,(2-amino-5-nitrophenyl)phenyl-
2-AMINO-5-NITROBENZOPHENONE, 98+%
2-AMINO-5-NITROBENZOPHENONE (DIAZEPAM)
5-Amino-2-nitrobenzophenone
Ro 7-1999
2-AMINO-5-NITROBENZOPHENONE=99.0%
Ro 7-19990
[EINECS(EC#)]

217-207-9
[Molecular Formula]

C13H10N2O3
[MDL Number]

MFCD00007364
[Molecular Weight]

242.23
[MOL File]

1775-95-7.mol
Chemical PropertiesBack Directory
[Appearance]

Yellow Solid
[Melting point ]

166-168 °C (lit.)
[Boiling point ]

385.05°C (rough estimate)
[density ]

1.2480 (rough estimate)
[refractive index ]

1.5300 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated)
[form ]

Solid
[pka]

-2.26±0.36(Predicted)
[color ]

Beige
[Water Solubility ]

3 mg/L (20 C)
[Usage]

A metabolite of Nitrazepam
[InChI]

InChI=1S/C13H10N2O3/c14-12-7-6-10(15(17)18)8-11(12)13(16)9-4-2-1-3-5-9/h1-8H,14H2
[InChIKey]

PZPZDEIASIKHPY-UHFFFAOYSA-N
[SMILES]

C(C1=CC([N+]([O-])=O)=CC=C1N)(C1=CC=CC=C1)=O
[CAS DataBase Reference]

1775-95-7(CAS DataBase Reference)
[NIST Chemistry Reference]

Methanone, (2-amino-5-nitrophenyl)phenyl-(1775-95-7)
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[RTECS ]

PC4935000
[REACH Registrations]

Active
[HS Code ]

29223990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Zinc chloride-->Benzoyl chloride-->Diphenylamine-->Benzophenone-->N-Methyl-4-nitroaniline-->4-Chlorobenzoic acid-->Acetamide, N-(2-benzoyl-4-nitrophenyl)--->Acetamide, 2-amino-N-(2-benzoyl-4-nitrophenyl)--->Methanone, (2-iodo-5-nitrophenyl)phenyl--->5-Nitroanthranilonitrile-->4'-Nitrobenzanilide-->2-Chloro-5-nitrobenzophenone-->2-Iodo-4-nitroaniline-->Phenylboronic acid
[Preparation Products]

Nitrazepam-->N-(2-benzoyl-4-nitrophenyl)-2-chloroacetamide-->4-Amino-3-nitrobenzophenone-->3-Acetyl-6-nitro-4-phenylquinolin-2(1H)-one
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2-Amino-5-nitrobenzophenone(1775-95-7).msds
Hazard InformationBack Directory
[Chemical Properties]

Yellow Solid
[Uses]

A metabolite of Nitrazepam
[Synthesis Reference(s)]

Synthetic Communications, 16, p. 485, 1986 DOI: 10.1080/00397918608057727
[General Description]

FT-IR and Raman spectra of 2-amino-5-nitrobenzophenone (ANBP) has been reported.
[Synthesis]

5-Nitroanthranilonitrile

17420-30-3

BENZENESULFINIC ACID SODIUM SALT

873-55-2

2-Amino-5-nitrobenzophenone

1775-95-7

2-Cyano-4-nitroaniline (0.3 mmol), sodium benzenesulfinate (0.6 mmol), palladium acetate (10 mol%), 2,2'-bipyridine (20 mol%), p-nitrobenzenesulfonic acid (10 equiv.), tetrahydrofuran (2 mL), and water (1 mL) were sequentially added to a Schlenk tube under the protection of nitrogen atmosphere. The reaction mixture was stirred vigorously at 80 °C for 48 hours. After completion of the reaction, the mixture was poured into ethyl acetate and washed sequentially with saturated sodium bicarbonate solution (2 x 10 mL) and saturated saline (1 x 10 mL). After the aqueous layer was extracted with ethyl acetate, all organic layers were combined and dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the residue was purified by fast column chromatography (eluent: hexane/ethyl acetate) to afford the target product 2-amino-5-nitrobenzophenone.

[References]

[1] Molecules, 2014, vol. 19, # 5, p. 6439 - 6449
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-5-nitrobenzophenone(1775-95-7)MS
2-Amino-5-nitrobenzophenone(1775-95-7)1HNMR
2-Amino-5-nitrobenzophenone(1775-95-7)13CNMR
2-Amino-5-nitrobenzophenone(1775-95-7)IR1
2-Amino-5-nitrobenzophenone(1775-95-7)IR2
2-Amino-5-nitrobenzophenone(1775-95-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Amino-5-nitrobenzophenone, 98%(1775-95-7)
[Alfa Aesar]

2-Amino-5-nitrobenzophenone, 98%(1775-95-7)
[Sigma Aldrich]

1775-95-7(sigmaaldrich)
[TCI AMERICA]

2-Amino-5-nitrobenzophenone,>98.0%(LC)(1775-95-7)
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