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Naphthalene, 1,4-difluoro-, also known as 1,4-difluoronaphthalene, is an organic compound with the chemical formula C10H6F2. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, where two hydrogen atoms are replaced by fluorine atoms at the 1 and 4 positions. Naphthalene, 1,4-difluoro- is characterized by its white crystalline appearance and is relatively stable. 1,4-difluoronaphthalene is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also a potential intermediate in the production of certain fluorinated materials. Due to its chemical structure, it exhibits different properties compared to its parent compound, naphthalene, such as altered reactivity and solubility.

315-52-6

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315-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315-52-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 315-52:
(5*3)+(4*1)+(3*5)+(2*5)+(1*2)=46
46 % 10 = 6
So 315-52-6 is a valid CAS Registry Number.

315-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-difluoronaphthalene

1.2 Other means of identification

Product number -
Other names 1,4-difluoro-naphthalene

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:315-52-6 SDS

315-52-6Downstream Products

315-52-6Relevant academic research and scientific papers

Fluorination of Bi- and polycyclic aromatic hydrocarbons with N-fluorobis(phenylsulfonyl)amine in the absence of solvent

Borodkin,Elanov,Shubin

experimental part, p. 1317 - 1322 (2011/01/04)

Reactions of N-fluorobis(phenylsulfonyl)amine with naphthalene, 1-methylnaphthalene, phenanthrene, anthracene, and pyrene without solvent were investigated. Sometimes the fluorination of aromatic compounds with N-fluorobis(phenylsulfonyl)amine without solvent proceeded more selectively than at the use of fluorinating reagents in solution.

Selective and efficient direct fluorination of polycyclic aromatic hydrocarbons using 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)

Stavber, Stojan,Zupan, Marko

, p. 1077 - 1078 (2007/10/03)

A new N-F fluorinating reagent 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Accufluor NFTh) was effectively used for selective fluorination of polycyclic aromatics. Naphthalene was site-selectively fluorinated to 1-fluoronaphthalene, phenanthrene to 9-fluorophenanthrene, and pyrene to 1-fluoropyrene. In a series of substituted naphthalenes the regioselectivity and effectiveness of fluorination depended on the position and the nature of the substituents.

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