5540-60-3

Basic information

• Product Name: N-(4-Chloro-3-nitrophenyl)acetamide
• Synonyms: 2-(4-Chloro-3-nitrophenyl)acetamide;Acetamide, N-(4-chloro-3-nitrophenyl)-;alpha-(4-Chloro-3-nitrophenyl)acetamide;4-CHLORO-3-NITROPHENYLACETAMIDE;3-NITRO-4-CHLOROACETANILIDE;3NC;A-(4-CHLORO-3-NITROPHENYL)ACETAMIDE;TIMTEC-BB SBB007993
• CAS NO: 5540-60-3
• Molecular Formula: C₈H₇ClN₂O₃
• Molecular Weight: 214.61
• EINECS: 226-904-7
• Product Categories: Intermediates of Dyes and Pigments;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 5540-60-3.mol
• Article Data: 17

Chemical Properties

• Melting Point: 147-148 °C
• Boiling Point: 404.1°Cat760mmHg
• Flash Point: 198.2°C
• Appearance: /
• Density: 1.466g/cm³
• Vapor Pressure: 1.99E-18mmHg at 25°C
• Refractive Index: 1.778
• PKA: 13.33±0.70(Predicted)
• CAS DataBase Reference: N-(4-Chloro-3-nitrophenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chloro-3-nitrophenyl)acetamide(5540-60-3)
• EPA Substance Registry System: N-(4-Chloro-3-nitrophenyl)acetamide(5540-60-3)

Safety Data

• Hazardous Substances Data: 5540-60-3(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 26, p. 1418, 1961 DOI: 10.1021/jo01064a022

InChI:InChI=1/C19H11NO5/c21-15-9-11(7-8-12(15)19(24)25)20-17(22)13-5-1-3-10-4-2-6-14(16(10)13)18(20)23/h1-9,21H,(H,24,25)

Upstream product

• 635-22-3 4-Chloro-3-nitroaniline 
• 108-24-7 acetic anhydride 
• 539-03-7 N-(4-chlorophenyl)acetamide 
• 106-47-8 4-chloro-aniline 
• 75-36-5 acetyl chloride 
• 122-28-1 N-(3-nitrophenyl)acetanilide 
• 64-19-7 acetic acid 

Downstream Products

• 74804-14-1 bis(4-acetylamino-2-nitrophenyl) disulphide 
• 56813-48-0 2-methylsulfanyl-benzothiazol-5-ylamine 
• 43087-91-8 2-phenyl-1,3-benzothiazol-5-amine 
• 857950-75-5 bis-(4-acetylamino-2-amino-phenyl)-disulfide 
• 857535-61-6 bis-(4-acetylamino-2-benzoylamino-phenyl)-disulfide 
• 108018-02-6 3'-amino-4'-mercaptoacetanilide 

Relevant articles and documents

Pyridine compound, preparation method and application thereof, and pharmaceutical composition

The invention provides a pyridine compound as well as a preparation method and application thereof, and belongs to the technical field of medical chemistry. The pyridine compound provided by the invention has excellent in-vitro antiviral activity and potential druggability, and is expected to become a clinical candidate molecule for overcoming influenza.

AZO COMPOUND, INK COMPOSITION, RECORDING METHOD AND COLORED MATERIAL

PROBLEM TO BE SOLVED: To provide a dye which has extremely excellent ozone gas resistance, extremely high print density, low color rendering property, and a high-quality black hue with low saturation, and to provide a black ink composition for inkjet recording containing the dye. SOLUTION: The present invention provides an azo compound represented by the following formula or a salt thereof [R1 is a C1-4 alkyl group or the like; R2 is a cyano group or the like; R5-R7 independently represent H, a C1-4 alkyl group, C1-4 alkoxy group or the like; R8-R10 independently represent H, a C1-4 alkylcarbonylamino group, C1-4 alkylthio group or the like; R11 is a C1-4 alkylthio group or the like; R12 and R13 independently represent H, a C1-8 alkylcarbonylamino group or the like; group A is a substituted naphthyl group]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

AZO COMPOUND, INK COMPOSITION, RECORDING METHOD AND COLORED MATTER

PROBLEM TO BE SOLVED: To provide a dye having a high-quality black hue with excellent gas resistance, printability, and color rendering properties, and a low saturation, and an inkjet recording black ink composition comprising the dye. SOLUTION: The present invention provides an azo compound represented by formula (1) or a tautomer thereof, or a salt thereof (R1 is a (C1-C4) alkyl group or the like; R2 is a cyano group; R3 and R4 independently represent H, a sulfo group or the like; R5 and R7 independently represent a (C1-C4) alkylthio group or the like; R6 and R8 independently represent a (C1-C4) alkylcarbonyl amino group; R9 is a sulfo (C1-C4) alkoxy group; R10 is a methyl group; R11-R13 are H, a sulfo group, or a nitro group; and at least one of R11-R13 is a nitro group). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT