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6-Fluorodibenz[a,h]anthracene is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C18H11F. It is a derivative of dibenz[a,h]anthracene, where one hydrogen atom is replaced by a fluorine atom. 6-Fluorodibenz[a,h]anthracene is known for its potential mutagenicity and carcinogenicity, similar to other PAHs, due to its ability to interact with DNA and cause mutations. It is not commonly found in the environment but can be synthesized for research purposes. The presence of fluorine in the molecule can affect its chemical properties, such as reactivity and stability, compared to the parent compound. Studies on 6-fluorodibenz[a,h]anthracene and related compounds contribute to understanding the effects of fluorination on the biological activity of PAHs.

1764-39-2

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1764-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1764-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1764-39:
(6*1)+(5*7)+(4*6)+(3*4)+(2*3)+(1*9)=92
92 % 10 = 2
So 1764-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H13F/c23-22-12-15-6-2-4-8-18(15)20-11-16-10-9-14-5-1-3-7-17(14)19(16)13-21(20)22/h1-13H

1764-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoronaphtho[1,2-b]phenanthrene

1.2 Other means of identification

Product number -
Other names 4-Fluor-1,2,5,6-dibenzo-anthracen

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:1764-39-2 SDS

1764-39-2Upstream product

1764-39-2Downstream Products

1764-39-2Relevant academic research and scientific papers

Pinpoint-fluorinated phenacenes: New synthesis and solubility enhancement strategies

Fuchibe, Kohei,Morikawa, Toshiyuki,Shigeno, Kento,Fujita, Takeshi,Ichikawa, Junji

supporting information, p. 1126 - 1129 (2015/03/14)

The Pd(II)-catalyzed cyclizations of 2,2-difluorovinylated biaryls, following a Friedel-Crafts-type mechanism, provide a new route to pinpoint-fluorinated phenacenes. The single fluorine substituent stabilized the synthesized fluoropicenes (fluoro[5]phenacenes) toward aerial oxidation and contributed to their solubility in organic solvents. For example, 6- and 13-fluoropicenes were 25- and 15-fold more soluble in THF than nonfluorinated picene. X-ray crystal structure analysis revealed that the fluorine substituent did not alter molecular planarity.

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