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1-Fluoronaphthalene

1-Fluoronaphthalene Structure
CAS No.
321-38-0
Chemical Name:
1-Fluoronaphthalene
Synonyms
Fluoronaphthalene;1-FLUORONAPTHALENE;1-Fluornaftalen;48720-u;NSC 4690;uoronaphthaL;Duloxetine-8;1-Fluoronaphth;Fluorophthalene;Duloxetine Imp-G
CBNumber:
CB8219439
Molecular Formula:
C10H7F
Molecular Weight:
146.16
MOL File:
321-38-0.mol
MSDS File:
SDS
Modify Date:
2024/7/24 17:31:20

1-Fluoronaphthalene Properties

Melting point -13 °C (lit.)
Boiling point 215 °C (lit.)
Density 1.1322 g/mL at 20 °C (lit.)
refractive index n20/D 1.593(lit.)
Flash point 150 °F
storage temp. Sealed in dry,Room Temperature
solubility slightly soluble in water, well soluble in chloroform, ethyl acetate, and methanol.
form Oil
color Colourless to Yellow
Specific Gravity 1.332
Water Solubility Not miscible or difficult to mix in water.
BRN 1906413
Stability Stable. Incompatible with strong oxidizing agents.
InChIKey CWLKTJOTWITYSI-UHFFFAOYSA-N
CAS DataBase Reference 321-38-0(CAS DataBase Reference)
NIST Chemistry Reference Naphthalene, 1-fluoro-(321-38-0)
EPA Substance Registry System 1-Fluoronaphthalene (321-38-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
RIDADR  UN2810
WGK Germany  3
RTECS  QJ7100000
Hazard Note  Flammable
TSCA  T
HazardClass  IRRITANT
HS Code  29039990
NFPA 704
2
1 0

1-Fluoronaphthalene price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 196657 1-Fluoronaphthalene 99% 321-38-0 5G ₹2574.2 2022-06-14 Buy
Sigma-Aldrich(India) 196657 1-Fluoronaphthalene 99% 321-38-0 25G ₹9442.25 2022-06-14 Buy
ALFA India ALF-A18378-22 1-Fluoronaphthalene, 98% 321-38-0 100g ₹29155 2022-05-26 Buy
TCI Chemicals (India) F0212 1-Fluoronaphthalene min. 98.0 % 321-38-0 5G ₹2700 2022-05-26 Buy
TCI Chemicals (India) F0212 1-Fluoronaphthalene min. 98.0 % 321-38-0 25G ₹6900 2022-05-26 Buy
Product number Packaging Price Buy
196657 5G ₹2574.2 Buy
196657 25G ₹9442.25 Buy
ALF-A18378-22 100g ₹29155 Buy
F0212 5G ₹2700 Buy
F0212 25G ₹6900 Buy

1-Fluoronaphthalene Chemical Properties,Uses,Production

Chemical Properties

clear slightly yellow to yellow-brown liquid

Uses

1-Fluoronaphthalene is a fluorinated naphthalene derivative that is metabolized by fungal monooxygenase-epoxide hydrolase. It is also used as a pharmaceutical intermediate. It is Duloxetine impurity.

Application

1-Fluoronaphthalene was used in t-BuLi-mediated synthesis of 6-substituted phenanthridines. It was also used in the synthesis of LY248686, a potent inhibitor of serotonin and norepinephrine uptake.

Preparation

The preparation of 1-Fluoronaphthalene is as follows:1) Diazotization reaction: 1500 g of hydrochloric acid (mass concentration: 25%) and 300 g of naphthylamine were added to a 3000 mL three-necked flask, stirred and heated to 75 ° C to dissolve, and the temperature was lowered to below 5 ° C, and 148 g was slowly added at this temperature. Sodium nitrite, stirred at low temperature for 0.3 hours after the addition, to obtain a diazonium salt solution;2) Substitution reaction: 360 g of fluoroboric acid solution (concentration: 45%) was added to the resulting solution obtained in the step 1), stirred for 0.25 h, filtered, and the filter cake was dried at a temperature of 50 ° C for 0.2 h to obtain Dry naphthylamine diazonium salt fluoroborate double salt;3) Hot air decomposition: the dried diazonium salt fluoroborate double salt is slowly added to the reactor through which hot air (hot air temperature is 85-90 ° C), and the dried powdered naphthylamine diazonium salt fluoroborate double salt is The hot air blows up the dispersion and absorbs the heat for thermal decomposition to obtain a 1-fluoronaphthalene solution containing a small amount of solid impurities;4) Purification treatment: the 1-fluoronaphthalene solution obtained in the step 3) is first washed with pure water for 3 to 6 times, then neutralized with a soda ash to a pH of 6.8 to 7.2, and finally the oil layer is separated by filtration, and the filtrate is taken. The distillation treatment gave 210 g of a naphthalene-based fluorine-containing intermediate 1-fluoronaphthalene in an amount of 99.8%.

321-38-0.png

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Simple aromatic halogenated organic compounds, such as Fluoronaphthalene, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

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