39905-57-2

Basic information

• Product Name: P-HEXYLOXYANILINE
• Synonyms: (p-hexyloxy)-anilin;4-(hexyloxy)-benzenamin;4-(hexyloxy)benzenamine;Aniline, (p-hexyloxy)-;4-N-HEXYLOXYANILINE;4-HEXYLOXYANILINE;AKOS BBB/081;P-HEXYLOXYANILINE
• CAS NO: 39905-57-2
• Molecular Formula: C₁₂H₁₉NO
• Molecular Weight: 193.29
• EINECS: 254-696-8
• Product Categories: Nitrogen Compounds;Organic Building Blocks;Alkylanilines;Amines;C11 to C38;Nitrogen Compounds;Building Blocks;C12;Chemical Synthesis
• Mol File: 39905-57-2.mol
• Article Data: 39

Chemical Properties

• Melting Point: 43-45 °C(lit.)
• Boiling Point: 155-158 °C5 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: White to brown/Solid
• Density: 0.9854 (rough estimate)
• Vapor Pressure: 0.000401mmHg at 25°C
• Refractive Index: 1.4596 (estimate)
• PKA: 5.26±0.10(Predicted)
• CAS DataBase Reference: P-HEXYLOXYANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: P-HEXYLOXYANILINE(39905-57-2)
• EPA Substance Registry System: P-HEXYLOXYANILINE(39905-57-2)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-28-36/37/39-45
• RIDADR: 2811
• WGK Germany: 3
• RTECS: BY2308000
• TSCA: Yes
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 39905-57-2(Hazardous Substances Data)

Usage

Uses

4-(Hexyloxy)aniline was used in the synthesis of 4-hydroxy-4′-hexyloxyazobenzene.

InChI:InChI=1/C12H19NO/c1-2-3-4-5-10-14-12-8-6-11(13)7-9-12/h6-9H,2-5,10,13H2,1H3

Upstream product

• 15440-98-9 1-(hexyloxy)-4-nitrobenzene 
• 111-25-1 1-bromo-hexane 
• 123-30-8 4-amino-phenol 
• 41240-77-1 N-(4-(hexyloxy)phenyl)acetamide 
• 636-98-6 p-nitrobenzene iodide 
• 111-27-3 hexan-1-ol 
• 103-90-2 4-acetaminophenol 
• 100-02-7 4-nitro-phenol 
• 824-78-2 4-nitrophenol sodium salt 
• 544-10-5 1-Chlorohexane 
• 638-45-9 1-Iodohexane 
• 1380548-22-0 C₁₆H₂₃NO₅ 

Downstream Products

• 102558-80-5 N-(4-hexyloxy-phenyl)-N',N''-di-[2]pyridyl-guanidine 
• 57666-62-3 5-(4-hexyloxy-phenyl)-furan-2-carbaldehyde 
• 104931-65-9 (4-Hexyloxy-phenyl)-[1-phenanthren-2-yl-meth-(E)-ylidene]-amine 
• 92524-24-8 [1-(9H-Fluoren-2-yl)-meth-(E)-ylidene]-(4-hexyloxy-phenyl)-amine 
• 98459-10-0 Benzoic acid 4-{[(E)-4-hexyloxy-phenylimino]-methyl}-phenyl ester 
• 141510-20-5 4-[2-[4-(hexyloxy)phenyl]diazen-1-yl]phenol 
• 918404-66-7 p-C₆H₁₃O-C₆H₄-CHN-C₆H₄-OC₆H₁₃-p 
• 319428-82-5 N-(4-hexyloxyphenyl)nicotinamide 
• 85429-71-6 4-hexyloxy-2'-pivalamido-4'-(2,4,6-triisopropylbenzenesulfonamido)diphenylamine 
• 1005179-13-4 C₂₄H₂₈N₂O₄ 

Relevant articles and documents

PHOTORESPONSIVE COMPOUND, AND ADHESIVE, TONER AND IMAGE FORMATION METHOD USING THE SAME

PROBLEM TO BE SOLVED: To provide a compound that is fluidized by light irradiation and is un-fluidized reversibly, and shows no excessive coloration. SOLUTION: The present invention relates to a compound of chemical formula 1a or 1b: R1 and r1 each denote a hydrogen atom, a halogen atom or the like; R2-R7 and r2-r7 each denote a group represented by chemical formula 2, a hydrogen atom, a halogen atom or the like, where at least one of R2-R7 and r2-r7 is a group represented by chemical formula 2; in chemical formula 2, X1 and X2 each denote N or CH, and X1≠X2; A1-A5 each denote a hydrogen atom, a halogen atom or the like, where at least one of A1-A5 is an alkyl group, an alkoxy group, an acyl group, an alkoxycarbonyl group, or an acyloxy group. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Discovery of Diphenoxy Derivatives with Flexible Linkers as Ligands for β-Amyloid Plaques

The highly rigid and planar scaffolds with π-conjugated systems have been widely considered to be indispensable for β-amyloid (Aβ) binding ligands. In this study, a library of diphenoxy compounds with different types of more flexible linkers as Aβ ligands were synthesized and evaluated. Most of them displayed good affinity (Ki1-42aggregates, and some ligands even showed values of Kiless than 10 nM. Structure-activity relationship analysis revealed that modification on the linkers or substituents tolerated great flexibility, which challenged the long-held belief that rigid and planar structures are exclusively favored for Aβ binding. Three ligands were labeled by iodine-125, and they exhibited good properties in vitro and in vivo, which further supported that this flexible scaffold was potential and promising for the development of Aβ imaging agents.

Structurally simple trimesic amides as highly selective anion channels

Trimesic amide molecules, which contain simple alkyl chains in their periphery, exhibit interesting anion-transport functions. The most active and highly selective channel TA12 efficiently transports ClO4? anions across membranes, with other anions conducted in the order of I? > NO3? > Br? > Cl?.