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24672-71-7

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24672-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24672-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24672-71:
(7*2)+(6*4)+(5*6)+(4*7)+(3*2)+(2*7)+(1*1)=117
117 % 10 = 7
So 24672-71-7 is a valid CAS Registry Number.

24672-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(4-bromophenyl)anthracene

1.2 Other means of identification

Product number -
Other names 9-(p-bromophenyl)anthracene

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:24672-71-7 SDS

24672-71-7Relevant articles and documents

PHOTOCHEMICAL VS. ELECTROCHEMICAL ELECTRON-TRANSFER REACTIONS. ONE-ELECTRON REDUCTION OF ARYL HALIDES BY PHOTOEXCITED ANION RADICALS.

Nelleborg, Palle,Lund, Henning,Eriksen, Jens

, p. 1773 - 1776 (1985)

Electrochemical reduction of aryl halides generally leads to expulsion of halide ion.The product aryl radical is unavoidably further reduced.In contrast, reduction of aryl halides by photoexcited anion radicals may be stopped at the aryl radical stage owing to the bimolecular nature of electron-transfer reactions.We have tested this hypothesis by photoinducing electron-transfer from anthraquinone anion radical to several aryl halides.For each halide it was possible to trap the corresponding radical by anthracene forming substituted 9-phenylanthracenes.

Photoreaction of anthracenyl phosphine oxides: Usual reversible photo- and heat-induced emission switching, and unusual oxidative P&C bond cleavage

Katagiri, Kosuke,Yamamoto, Yukina,Takahata, Yuui,Kishibe,Fujimoto

supporting information, p. 2026 - 2029 (2019/07/03)

Anthracenyl(diphenyl)phosphine oxide and dianthracenylphenylphosphine oxide as photoactive compounds have been synthesized. Anthracenyl group of these compounds indicate the multi-functional roles such as an emission component, a photodimerization component, and a leaving group. When the light irradiation was performed under an oxygen atmosphere, photo-oxidative P&C bond cleavage to leave the antharacenyl group was observed. Moreover, phosphonyl radical was produced and then P&P bond formation to form diphosphane was observed.

Semiconducting Material Comprising a Phosphine Oxide Matrix and Metal Salt

-

, (2018/05/03)

The present invention is directed to a semiconducting material comprising: i) a compound according to formula (I) wherein R1, R2 and R3 are independently selected from C1-C30-alkyl, C3-C30 cycloalkyl, C2-C30-heteroalkyl, C6-C30-aryl, C2-C30-heteroaryl, C1-C30-alkoxy, C3-C30-cycloalkyloxy, C6-C30 aryloxy, and from structural unit having general formula E-A-, wherein—A is a C6-C30 phenylene spacer unit, and—E is an electron transporting unit that is selected from C10-C60 aryl and C6-C60 heteroaryl comprising up to 6 heteroatoms independently selected from O, S, P, Si and B and that comprises a conjugated system of at least 10 delocalized electrons, and—at least one group selected from R1, R2 and R3 has the general formula E-A-; and ii) at least one complex of a monovalent metal having formula (II) wherein—M+ is a positive metal ion bearing a single elementary charge, and each of A1, A2, A3 and A4 is independently selected from H, substituted or unsubstituted C6-C20 aryl and substituted or unsubstituted C2-C20 heteroaryl, wherein a heteroaryl ring of at least 5 ring-forming atoms of the substituted or unsubstituted C2-C20 heteroaryl comprises at least one hetero atom selected from O, S and N.

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