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Anthracene, 9-(pentyloxy)-, also known as 9-Pentyloxyanthracene, is an organic compound with the chemical formula C19H22O. It is a derivative of anthracene, a polycyclic aromatic hydrocarbon, with a pentyloxy group attached at the 9-position. Anthracene, 9-(pentyloxy)- is characterized by its planar structure and conjugated π-electron system, which contributes to its unique electronic and optical properties. It is often used in the synthesis of various organic compounds and as a building block in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and other optoelectronic devices. The presence of the pentyloxy group influences the compound's solubility and reactivity, making it a versatile intermediate in organic synthesis.

112607-81-5

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112607-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112607-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,0 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112607-81:
(8*1)+(7*1)+(6*2)+(5*6)+(4*0)+(3*7)+(2*8)+(1*1)=95
95 % 10 = 5
So 112607-81-5 is a valid CAS Registry Number.

112607-81-5Downstream Products

112607-81-5Relevant academic research and scientific papers

Synthesis of 9-anthryl ethers from trans-9,10-dihydro-9,10- dimethoxyanthracene by acid-catalyzed transetherification

Keun, Sam Jang,Hee, Young Shin,Dae, Yoon Chi

experimental part, p. 1703 - 1707 (2009/12/24)

During a study of electrophilic aromatic addition reactions (Ad EAr) to anthracene, anthryl ethers at the C9-position of anthracene were obtained as the major products when trans-9,10-dihydro-9,10- dimethoxyanthracene was reacted (10 minutes at

Application of Lanthanoids to Organic Chemistry. Direct Alkoxylation of Anthracene

Sugiyama, Takashi

, p. 1013 - 1016 (2007/10/02)

Direct alkoxylation of anthracene with some lower alcohols and ethylene glycol monoalkyl ethers, or monoacetate were carried out in the presence of cerium(IV)tetrakis(trifluoro acetate), and expected alkoxylated anthracene derivatives were obtained.

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