26697-35-8

Basic information

• Product Name: 4-BENZYLOXY-2-NITROANILINE
• Synonyms: 4-BENZYLOXY-2-NITROANILINE;2-Nitro-4-(benzyloxy)aniline;(4-Benzyloxy-2-nitrophenyl)aMine;2-Nitro-4-(phenylMethoxy)benzenaMine;Aniline, 4-(benzyloxy)-2-nitro- (8CI);NSC 93775;2-nitro-4-phenylMethoxyaniline;4-(benzyloxy)-2-nitrobenzenamine
• CAS NO: 26697-35-8
• Molecular Formula: C₁₃H₁₂N₂O₃
• Molecular Weight: 244.24598
• Product Categories: Aromatics Compounds;Aromatics;Amines
• Mol File: 26697-35-8.mol
• Article Data: 14

Chemical Properties

• Melting Point: 141-143°C
• Boiling Point: 443.6°C at 760 mmHg
• Flash Point: 222.1°C
• Appearance: /
• Density: 1.297g/cm³
• Vapor Pressure: 4.59E-08mmHg at 25°C
• Refractive Index: 1.644
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Dichloromethane, Ethyl Acetate, Methanol
• PKA: 0.90±0.10(Predicted)
• CAS DataBase Reference: 4-BENZYLOXY-2-NITROANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BENZYLOXY-2-NITROANILINE(26697-35-8)
• EPA Substance Registry System: 4-BENZYLOXY-2-NITROANILINE(26697-35-8)

Safety Data

• Hazardous Substances Data: 26697-35-8(Hazardous Substances Data)

Usage

Chemical Properties

Red Solid

InChI:InChI=1/C13H12N2O3/c14-12-7-6-11(8-13(12)15(16)17)18-9-10-4-2-1-3-5-10/h1-8H,9,14H2

Upstream product

• 26697-34-7 N-(4-(benzyloxy)-2-nitrophenyl)acetamide 
• 610-81-1 4-hydroxy-2-nitroaniline 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 41927-14-4 N-[4-(benzyloxy)phenyl]acetamide 
• 100-51-6 benzyl alcohol 
• 103-90-2 4-acetaminophenol 

Downstream Products

• 41927-17-7 4-(benzyloxy)-1,2-phenylenediamine 
• 238405-67-9 4-benzyloxy-2-nitrobenzenesulfonyl chloride 
• 755026-51-8 methyl 2-{[4-(benzyloxy)-2-nitrophenyl]amino}-4-chlorobenzoate 
• 755026-52-9 methyl 2-(2-amino-4-(benzyloxy)phenylamino)-4-chlorobenzoate 
• 894763-36-1 {[2-(bis-ethoxycarbonylmethyl-amino)-5-formyl-4-hydroxy-phenyl]-ethoxycarbonylmethyl-amino}-acetic acid ethyl ester 
• 894763-34-9 {[5-benzyloxy-2-(bis-ethoxycarbonylmethyl-amino)-phenyl]-ethoxycarbonylmethyl-amino}-acetic acid ethyl ester 
• 894763-35-0 {[5-benzyloxy-2-(bis-ethoxycarbonylmethyl-amino)-4-formyl-phenyl]-ethoxycarbonylmethyl-amino}-acetic acid ethyl ester 
• 894763-37-2 2-{(2-{bis-[(2-hydroxy-ethylcarbamoyl)-methyl]-amino}-4-formyl-5-hydroxy-phenyl)-[(2-hydroxy-ethylcarbamoyl)-methyl]-amino}-N-(2-hydroxy-ethyl)-acetamide 
• 238406-39-8 methyl 2(R)-2-(1,1-dioxido-7-phenyl-4,5-dihydro-1,2,5-benzothiadiazepin-2(3H)-yl)propanoate 
• 529496-51-3 2-(1,1-dioxo-7-phenoxy-1,3,4,5-tetrahydro-1λ⁶-benzo[f][1,2,5]thiadiazepin-2-yl)-propionic acid methyl ester 
• 238405-68-0 N-(4-benzyloxy-2-nitrobenzenesulfonyl)-D-alanine methyl ester 
• 238405-71-5 methyl 2(R)-[7-benzyloxy-2,3,4,5-tetrahydrobenzo[1,2,5-f]thiadiazepine-1,1-dioxide]propanoate 
• 529496-50-2 2-[7-(4-methoxy-phenoxy)-1,1-dioxo-1,3,4,5-tetrahydro-1λ⁶-benzo[f][1,2,5]thiadiazepin-2-yl]-propionic acid methyl ester 
• 1026153-59-2 2-(4-benzyloxy-2-nitro-benzenesulfonylamino)-3-methyl-butyric acid tert-butyl ester 

Relevant articles and documents

INHIBITORS OF ENL/AF9 YEATS

Methods and compositions for treating leukemia are disclosed. Acylated 6-aminoindoles, acylated 6-aminopyrrolopyridines and acylated 3-aminopyrrolo[3,2-c]pyridazines of the following formula inhibit ENL/AF9 YEATS and are therefore useful for treating leukemia.

Disperse scarlet dye compound, preparation method therefor and application of disperse scarlet dye compound

The invention discloses a disperse scarlet dye compound, a preparation method therefor and an application of the disperse scarlet dye compound. The disperse scarlet dye compound has a structure represented by a formula (I) shown in the description, wherein R is alkyl, alkoxy, halogen, nitro, cyano, a formula shown in the description or -OCH2CH=CH2. The invention provides the application of the disperse scarlet dye compound in printing and dyeing of hydrophobic textile materials. The disperse scarlet dye compound is bright-colored and beautiful in color and luster and has excellent washing fastness and sublimation fastness.

Functionalized alkoxy arene diazonium salts from paracetamol

Arene diazonium tetrafluoroborates can be synthesized from aromatic acetamides via a sequence of deacetylation, diazotation and precipitation, induced by anion exchange. The reaction is conducted as a convenient one-flask transformation with consecutive addition of the appropriate reagents. Exchange of solvents or removal of byproducts prior to isolation of the product is not required. The arene diazonium salts are isolated from the reaction mixture by simple filtration. Two complementary protocols are presented, and the utility of the reaction is exemplified for a synthesis of the diarylheptanoid natural product de-O-methyl centrolobine.