10472-97-6

Basic information

• Product Name: 8-PHENYL-1-OCTANOL
• Synonyms: 8-PHENYL-N-OCTANOL;8-PHENYLOCTANOL;8-PHENYL-1-OCTANOL;8-PHENYLOCTANOL 97%;8-Phenyloctyl alcohol;8-phenyloctan-1-ol;Benzeneoctanol
• CAS NO: 10472-97-6
• Molecular Formula: C₁₄H₂₂O
• Molecular Weight: 206.32
• Mol File: 10472-97-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 126-128°C 0,2mm
• Flash Point: 125-127°C/0.2mm
• Appearance: colourless liquid
• Density: 0.942 g/mL at 20 °C
• Vapor Pressure: 0.0001mmHg at 25°C
• Refractive Index: 1.5060
• PKA: 15.20±0.10(Predicted)
• Water Solubility: Not miscible or difficult to mix with water.
• Stability: Stable. Incompatible with strong oxidizing agents. Combustible.
• BRN: 2556146
• CAS DataBase Reference: 8-PHENYL-1-OCTANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 8-PHENYL-1-OCTANOL(10472-97-6)
• EPA Substance Registry System: 8-PHENYL-1-OCTANOL(10472-97-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-36/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 10472-97-6(Hazardous Substances Data)

Usage

Chemical Properties

colourless liquid

InChI:InChI=1/C14H22O/c15-13-9-4-2-1-3-6-10-14-11-7-5-8-12-14/h5,7-8,11-12,15H,1-4,6,9-10,13H2

Upstream product

• 26547-51-3 8-phenyloctanoic acid 
• 637-59-2 1-Bromo-3-phenylpropane 
• 5631-95-8 2,3-dichlorotetrahydro-2H-pyran 
• 502929-58-0 8-phenyl-7-octenyl tetrahydropyranyl ether 
• 502929-60-4 8-phenyloctyl tetrahydropyranyl ether 
• 201230-82-2 carbon monoxide 
• 536-74-3 phenylacetylene 
• 100863-10-3 trans-8-Phenyl-octen-⁽⁴⁾-ol-⁽¹⁾ 

Downstream Products

• 54646-75-2 1-bromo-8-phenyloctane 
• 62116-89-6 8-phenyl-octanal 
• 1334648-21-3 N(α)-[(1,1-dimethylethoxy)carbonyl]-N(?)-(8-phenyloctyl)-L-histidine methyl ester 
• 100-52-7 benzaldehyde 
• 1094765-49-7 3-(4-chlorophenyl)-2-(4-(8-azidooctylphenyl)thiazol-2-ylamino)propionic acid 
• 1094765-51-1 3-(4-chlorophenyl)-2-(4-(8-aminooctylphenyl)thiazol-2-ylamino)propionic acid 
• 1094765-46-4 2-bromo-4'-(8-azido-octyl)acetophenone 
• 1094765-44-2 C₁₆H₂₃N₃O 

Relevant articles and documents

PRODUCTS OF THE CATALYZED SYNTHESIS OF AROMATIC ALCOHOLS FROM PHENYLACETYLENE, CARBON MONOXIDE, AND HYDROGEN

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Controlled semihydrogenation of aminoalkynes using ethylenediamine as a poison of Lindlar's catalyst

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Quaternary ammonium compounds having muscle relaxation activity

A quaternary ammonium having a muscle relaxation activity compound represented by the formula (I): STR1 wherein R1 represents a methylene, a lower alkylenoxy, a lower alkenylene, a lower alkynylene, --CO--, --COO--, a lower alkylene carbonyloxy, --CH(OR5)--, a lower alkylenecarbonyl, a hydroxy lower alkylene, --O--, --S--, --SO--, or --SO2 --; R2 represents a hydrogen atom, a hydroxy lower alkyl, an aldehyde, a lower alkyl carbonyl, --NO2, or --NHR6 ; R3 represents a hydrogen atom of a group --R1 --(CH2)a --[CH(CH2 A)--CH2 ]b --A; R4 represents an anion; R5 and R6 represent a hydrogen atom or a acetyl; A represents a quaternary ammonium group; a represents an integer of 1 to 8; b represents 0 or 1; m represents an integer of 1 to 4; and (Z) represents a trivalent benzene ring, a trivalent naphthalene ring, a trivalent diphenyl or a trivalent ethane radical.