128915-32-2

Basic information

• Product Name: 3,5-DICHLORO-N-(4-NITROPHENYL)BENZENECARBOXAMIDE
• Synonyms: 3,5-DICHLORO-N-(4-NITROPHENYL)BENZENECARBOXAMIDE
• CAS NO: 128915-32-2
• Molecular Formula: C₁₃H₈Cl₂N₂O₃
• Molecular Weight: 311.12
• Mol File: 128915-32-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 405.8±45.0 °C(Predicted)
• Appearance: /
• Density: 1.524±0.06 g/cm3(Predicted)
• PKA: 11.27±0.70(Predicted)
• CAS DataBase Reference: 3,5-DICHLORO-N-(4-NITROPHENYL)BENZENECARBOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DICHLORO-N-(4-NITROPHENYL)BENZENECARBOXAMIDE(128915-32-2)
• EPA Substance Registry System: 3,5-DICHLORO-N-(4-NITROPHENYL)BENZENECARBOXAMIDE(128915-32-2)

Safety Data

• Hazardous Substances Data: 128915-32-2(Hazardous Substances Data)

Upstream product

• 128915-06-0 N¹⁶-(3,5-dichlorobenzoyl)-N¹,N²-di(p-nitrophenyl)formamidine 
• 622-57-1 N-ethyl-p-tolylamine 
• 51-36-5 3,5-dichlorobenzoic acid 
• 6575-00-4 3,5-dichlorobenzonitrile 
• 2905-62-6 3,5-dichlorobenzoyl chloride 
• 100-01-6 4-nitro-aniline 
• 2232-13-5 N¹,N²-di(p-nitrophenyl)formamidine 

Relevant articles and documents

Synthesis of Dichlorobenzamide Derivatives: Crystal Structures of 3,5-Dichloro-N-(2-chlorophenyl)benzamide and 3,5-Dichloro-N-(4-chlorophenyl)benzamide

Abstract: Reactions of 3,5-dichlorobenzoyl chloride and arylamine compounds in N,N′-dimethylformamidesolution at 60 °C afforded a series of dichlorobenzamidederivatives 4–14 in good yields. These new compounds and accompanyingintermediates were characterized and confirmed by nuclear magneticresonance and infrared spectroscopy, of which structures of compounds 4and 6 were established by X-ray crystallography. Compound 4 crystallizesin triclinic space group Pī, with a = 5.047 (18), b = 10.28 (4), c = 13.36 (5) ?, α =107.59 (5)°, β = 93.55 (5)°, γ = 98.34 (5)°, and Z = 2. The unit cell of 6 has a monoclinic Pn symmetry with the cell parameters a = 9.581 (3), b = 12.217 (4), c = 11.072 (3) ?, β = 92.584 (4)°, and Z = 4. Graphic Abstract: A series of 3,5-dichlorobenzamide compounds were synthesized from reactions of arylamine compounds with 3,5-dichlorobenzoyl chloride, which was prepared from 3,5-dichlorobenzonitrile.[Figure not available: see fulltext.]

Amidines. II. Preparation of unsymmetrical N1,N2-disubstituted amidines

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