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Acenaphtho[1,2-j]fluoranthe is a polycyclic aromatic hydrocarbon (PAH) consisting of a naphthalene and fluoranthene fused together. It is a complex organic molecule with a molecular formula of C20H12 and a molecular weight of 252.31 g/mol. Acenaphtho[1,2-j]fluoranthe is characterized by its unique structure, which features a benzene ring fused to a naphthalene and fluoranthene system. Acenaphtho[1,2-j]fluoranthe is a member of the PAH family, which are known for their potential carcinogenic and mutagenic properties. Due to its complex structure and potential health risks, research on Acenaphtho[1,2-j]fluoranthe is essential for understanding its environmental and health impacts.

193-21-5

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193-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193-21-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 193-21:
(5*1)+(4*9)+(3*3)+(2*2)+(1*1)=55
55 % 10 = 5
So 193-21-5 is a valid CAS Registry Number.

193-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Acenaphtho[1,2-j]fluoranthene

1.2 Other means of identification

Product number -
Other names 10,11-(peri-Naphthylen)-fluoranthen

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:193-21-5 SDS

193-21-5Downstream Products

193-21-5Relevant academic research and scientific papers

Construction of new fluorophores by Diels-Alder reaction of diacenaphthothiophenes

Yamamoto, Yuma,Fukuoka, Yoshiaki,Nishida, Jun-ichi,Kitamura, Chitoshi,Kawase, Takeshi

, p. 5725 - 5730 (2017/08/26)

The Diels–Alder (DA) reaction of diacenaphtheno[1,2-b;1′,2′-d]thiophene (1a) with benzyne affords 1:1 and 1:2 adducts, 7 and 8, in 47 and 11% yields. An X-ray crystallographic analysis reveals that 8 possesses a dibenzobarrelene structure involving a rigi

Synthesis of substituted benzene derivatives by homo- and hetero-coupling of 2-bromobenzaldehyde and bromovinylaldehydes followed by McMurry coupling

Some, Surajit,Dutta, Bishnupada,Ray, Jayanta K.

, p. 1221 - 1224 (2007/10/03)

A convenient synthetic approach to substituted benzene derivatives by modified Ullmann cross-coupling of 2-bromobenzaldehyde and bromovinylaldehydes followed by intramolecular McMurry coupling has been developed.

Study of structural aspects of thermochemical conversions of compounds modeling oligophenylenes containing acenaphthylenyl and acenaphthenyl groups

Kovalev, A. I.,Balykova, T. N.,Lindeman, S. V.,Teplyakov, M. M.,Khotina, I. A.,et al.

, p. 790 - 798 (2007/10/02)

With the aim of elucidating the mechanism of the thermochemical conversion of oligophenylenes containing acenaphthylenyl groups, the thermolysis of model compounds: 1,3,5-tris(5-acenaphthylenyl)benzene (1), 1,3,5-tris(5-acenaphthenyl)benzene (2), acenaphthylene, and acenaphthene, was studied by differential thermal analysis (DTA), dynamic thermogravimetric analysis (TGA), and mass spectrometry.Compounds 1 and 2 were studied by X-ray structural analysis.A scheme for the formation of secondary structures was suggested.Optimum temperature conditions were found for preparing thermostable, heat-resistant, and stable to thermooxidation polymers based on compounds containing the acenaphthylenyl groups. - Key words: 1,3,5-tris(acenaphthylenyl)benzene, 1,3,5-tris(acenaphthenyl)benzene, acenaphthylene, acenaphthene, thermochemical conversions; decacyclene; polymers, thermal properties; X-ray structural analysis.

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