119489-67-7

Basic information

• Product Name: 3-(HEPTADECAFLUOROOCTYL)ANILINE
• Synonyms: Benzenamine,3-(heptadecafluorooctyl)- (9CI)
• CAS NO: 119489-67-7
• Molecular Formula: C₁₄H₆F₁₇N
• Molecular Weight: 511.18
• Mol File: 119489-67-7.mol

Chemical Properties

• Melting Point: 33-38 °C
• Boiling Point: 271.1°C at 760 mmHg
• Flash Point: 120.5°C
• Appearance: /
• Density: 1.61g/cm³
• Vapor Pressure: 0.00659mmHg at 25°C
• Refractive Index: 1.359
• BRN: 6023253
• CAS DataBase Reference: 3-(HEPTADECAFLUOROOCTYL)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(HEPTADECAFLUOROOCTYL)ANILINE(119489-67-7)
• EPA Substance Registry System: 3-(HEPTADECAFLUOROOCTYL)ANILINE(119489-67-7)

Safety Data

• WGK Germany: 3
• F: 10-23
• Hazardous Substances Data: 119489-67-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H6F17N/c15-7(16,5-2-1-3-6(32)4-5)8(17,18)9(19,20)10(21,22)11(23,24)12(25,26)13(27,28)14(29,30)31/h1-4H,32H2

Upstream product

• 507-63-1 1-iodoheptadecafluorooctane 
• 626-01-7 3-Iodoaniline 

Downstream Products

• 120606-37-3 isothiocyanato-3-(n-perfluorooctyl)benzene 
• 325459-90-3 1-Bromo-3-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)benzene 
• 325459-91-4 (C₆H₄(C₈F₁₇))3P 
• 326806-85-3 N-allyl-3-perfluorooctylbenzenamine 
• 326806-83-1 N-[3-(perfluorooctyl)phenyl]-2,4-dinitrobenzenamine 

Relevant articles and documents

Synthesis and catalytic activity of fluorous chiral primary amine-thioureas

Three enantiopure fluorous thioureas featuring a free -NH2 group were synthesized by direct addition of aromatic isothiocyanates bearing a single n-C8F17 substituent in the ortho, meta and para position, respectively, to e

Materials for inducing alignment in liquid crystal and liquid crystal displays

The present invention provides novel aromatic diamines useful in preparing polyimides for optical alignment layers in liquid crystal displays. The novel compositions comprise side-chains general formula I -L1-D-L2-Cf wherein D comprises 1 to 4 carbon-carbon double bonds, Cf is a monovalent C4 to C20 fluorocarbon radical and L1 and L2 are linking groups.

LANGMUIR-BLODGETT FILMS OF POLYALLYLAMINE MODIFIED WITH (PERFLUOROALKYL)PHENYL GROUPS

(Perfluoroalkyl)phenyl groups were introduced to polyallylamine by thiourea bonds.Langmuir-Blodgett (LB) films of the polymers were successfully prepared.Characterization of the films indicated that structural isomerism of substituted benzene has an effect upon the molecular ordering in the LB film and that the limiting area and critical surface tension of the LB films become smaller in the order, ortho, meta, and para isomers.