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9-Dodecylanthracene is an organic compound with the chemical formula C20H26. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, where a dodecyl (C12H25) alkyl chain is attached to the 9th carbon position. 9-Dodecylanthracene is characterized by its waxy appearance and is insoluble in water but soluble in organic solvents. It is used in various applications, including as a fluorescent probe in biochemistry and as a component in organic light-emitting diodes (OLEDs) due to its ability to emit light when excited. The presence of the long alkyl chain influences its solubility and stability, making it a versatile molecule in chemical research and technology.

2883-70-7

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2883-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2883-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2883-70:
(6*2)+(5*8)+(4*8)+(3*3)+(2*7)+(1*0)=107
107 % 10 = 7
So 2883-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C26H34/c1-2-3-4-5-6-7-8-9-10-11-20-26-24-18-14-12-16-22(24)21-23-17-13-15-19-25(23)26/h12-19,21H,2-11,20H2,1H3

2883-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-dodecylanthracene

1.2 Other means of identification

Product number -
Other names Anthracene,9-dodecyl

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:2883-70-7 SDS

2883-70-7Relevant academic research and scientific papers

FUNCTIONALIZED ANTHRACENE-CAPPED OLIGOTHIOPHENES AND ORGANIC SEMICONDUCTORS BASED ON THE SAME, USE THEREOF

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Page/Page column 22, (2012/06/30)

The present invention relates to a series of compounds having functionalized anthracene-capped oligothiophenes and its derivatives and the organic semiconductor device using the same, in particular, organic field-effect transistors (OFETs) comprising the above compounds.

Reactions of Haloarenes with Thiolate Anions in Tetraglyme: Cmpetition between Electron Transfer and SNAr Mechanisms

Pastor, Stephen D.

, p. 859 - 866 (2007/10/02)

The reaction of the bromo-substituted naphthalene 1 with the alkanethiolate anions 2a-b and arenethiolate 2c in tetraglyme gave the corresponding 1-naphthyl thio-ethers 3a-c.Thio-ethers 3a-c were oxidized to the corresponding sulfones 4a-c with m-chloroperoxybenzoic acid.The reaction of the dichloro-substituted anthracene 5a with 2b gave the disubstitution product 6a.The reaction of 9-bromoanthracene 5c with the alkanethiolate 2b gave 6b, whereas the reaction of 5c with the arenethiolate 2c gave a mixture of aubstitution product 6c and anthracene 7.The observation of the formation of both 6c and 7 is explained by the competition between substitution (SNAr) and electron-transfer (ET) mechanisms.Consistent with this interpretation, the reaction of the monochloro-substituted 5b, which has a higher-energy ?* orbital, with 2c gave 6c without the formation of 7.Zn/KOH in tetraglyme was shown to reduce the aryl halides 5b-c and thio-ether 6c to 7.

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