Nitroacetanilide
{{refimprove|date=March 2015}}
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 424674028
| Reference =
| Name = 4-Nitroacetanilide
| ImageFile = 4-Nitroacetanilide.svg
| PIN = N-(4-Nitrophenyl)acetamide
| OtherNames = p-Acetamidonitrobenzene; p-Nitroacetanilide; N-Acetyl-4-nitroaniline
| Section1 = {{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 104-04-1
| ChEMBL = 131469
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = PH3B066365
| RTECS =
| EINECS = 203-169-0
| UNNumber =
| PubChem = 7691
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 7407
| SMILES = O=C(Nc1ccc(cc1)[N+]([O-])=O)C
| InChI = 1/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)
| InChIKey = NQRLPDFELNCFHW-UHFFFAOYAB
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = NQRLPDFELNCFHW-UHFFFAOYSA-N
}}
| Section2 = {{Chembox Properties
| Formula = C8H8N2O3
| MolarMass = 180.16 g/mol
| Appearance = Solid, white-green or brown
| Density = 1.34 g/cm3
| Solubility =
| MeltingPtC = 215
| BoilingPtC = 408.9
| Viscosity =
| pKa =
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| Section3 =
| Section4 =
| Section5 =
| Section6 =
| Section7 = {{Chembox Hazards
| MainHazards = Irritant
| ExternalSDS =
| FlashPt =
| NFPA-H =
| NFPA-F =
| NFPA-R =
| NFPA-S =
| GHSPictograms = {{GHS07}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|315|319|335}}
| PPhrases = {{P-phrases|261|264|271|280|302+352|304+340|305+351+338|312|332+313|337+313|362|403+233|405|501}}
}}
| Section8 = {{Chembox Related
| OtherFunction_label =
| OtherFunction =
| OtherCompounds =
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File:Deacylation of Nitroacetanilide.jpg
4-Nitroacetanilide is a chemical compound which is a nitro derivative of acetanilide. There are two other isomers of nitroacetanilide, 2-nitroacetanilide and 3-nitroacetanilide.
4-Nitroacetanilide is used as in intermediate in the production of some dyes."Dyes and Dye Intermediates" in Kirk‑Othmer Encyclopedia of Chemical Technology, Peter Gregory, {{doi|10.1002/0471238961.0425051907180507.a01}}