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Acenaphthylene, 3-fluoro-1,2-dihydro- is a chemical compound with the molecular formula C12H9F. It is a derivative of acenaphthylene, a polycyclic aromatic hydrocarbon, with a fluorine atom attached to the 3-position of the molecule. This fluorinated compound is of interest in chemical research due to its potential applications in the synthesis of various pharmaceuticals and materials. The presence of the fluorine atom can significantly alter the physical and chemical properties of the molecule, such as its reactivity, stability, and lipophilicity, which can be crucial in drug design and material science. The compound is typically synthesized through various chemical reactions and is used as an intermediate in the production of more complex molecules.

3798-80-9

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3798-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3798-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3798-80:
(6*3)+(5*7)+(4*9)+(3*8)+(2*8)+(1*0)=129
129 % 10 = 9
So 3798-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H9F/c13-11-7-5-9-3-1-2-8-4-6-10(11)12(8)9/h1-3,5,7H,4,6H2

3798-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-fluoro-1,2-dihydroacenaphthylene

1.2 Other means of identification

Product number -
Other names 3-fluoroacenaphthalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3798-80-9 SDS

3798-80-9Downstream Products

3798-80-9Relevant academic research and scientific papers

Fluorination with Xenon Difluoride. 23. Fluorination of Ortho Substituted Aromatic Molecules

Sket, Boris,Zupan, Marko

, p. 279 - 281 (1981)

The fluorination of 9,10-dihydroxyanthracene and triptycene with xenon difluoride in the presence of hydrogen fluoride occured at α and β position with β attack predominating over α attack, while the reaction with acenaphthalene resulted in the formation of 2- and 4-fluorosubstituted products, regioselectivity being very little affected by the nature of the catalyst: hydrogen fluoride, boron trifluoride and pentafluorothiophenol.The fluorination of 1,2,3,4-tetrahydro-1,4-methanonaphthalene resulted in the formation of 6-fluoro-1,2,3,4-tetra-hydro-1,4-methanonaphthalene, 6,7-difluoro-1,2,3,4-tetrahydro-1,4-methanonaphthalene and rearranged product 1-(2,2-difluoroethyl)indan.

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