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1,2-di(1-H-pyrrol-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

178461-72-8

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178461-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178461-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178461-72:
(8*1)+(7*7)+(6*8)+(5*4)+(4*6)+(3*1)+(2*7)+(1*2)=168
168 % 10 = 8
So 178461-72-8 is a valid CAS Registry Number.

178461-72-8Downstream Products

178461-72-8Relevant academic research and scientific papers

Improved Synthesis of ortho-Phenylene-bridged Cyclic Tetrapyrroles and Oxidative Fusion Reactions Toward Substituted Tetraaza[8]circulenes

Morimoto, Yuki,Chen, Fengkun,Matsuo, Yusuke,Kise, Koki,Tanaka, Takayuki,Osuka, Atsuhiro

, p. 648 - 655 (2021)

Hetero[8]circulenes have emerged as novel functionalized heteronanographenes that show various promising functions such as bright fluorescence, charge transporting, and redox reactivities. One of the effective synthetic strategy is the fold-in type oxidat

Facile synthesis of indolizino[3,4,5-ab]isoindoles by an acid-induced cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes

Kuzuhara, Daiki,Miyake, Satoshi,Moriyama, Hirotake,Tamura, Yuto,Aratani, Naoki,Yamada, Hiroko

, p. 5564 - 5567 (2015)

The new synthetic method of indolizino[3,4,5-ab]isoindoles (INIs) by an acid-induced intramolecular cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes has been developed. This protocol can be applied to the preparation of INI derivatives with electron-donating and -withdrawing groups as well as azaINIs.

Synthesis of a Tetrabenzotetraaza[8]circulene by a "fold-In" Oxidative Fusion Reaction

Chen, Fengkun,Hong, Yong Seok,Shimizu, Soji,Kim, Dongho,Tanaka, Takayuki,Osuka, Atsuhiro

, p. 10639 - 10642 (2015)

Tetrabenzotetraaza[8]circulene (1) has been synthesized in good yield by a "fold-in" oxidative fusion reaction of a 1,2-phenylene-bridged cyclic tetrapyrrole. X-ray diffraction analysis of 1 has revealed a planar square structure with a central cyclooctat

Calix[2]bispyrrolylarenes: New expanded calix[4]pyrroles for fluorometric sensing of anions via extended π-conjugation

Chandra, Brijesh,Mahanta, Sanjeev P.,Pati, Narendra N.,Baskaran, Sambath,Kanaparthi, Ravi K.,Sivasankar, Chinnappan,Panda, Pradeepta K.

, p. 306 - 309 (2013)

Two new expanded calix[4]pyrroles 3 and 4 were synthesized by '2 + 2' cyclocoupling of easily prepared diboryldipyrromethane 7 (by Ir-catalyzed CH-bond activation) with appropriate diiodoarenes using the Suzuki protocol. Owing to the unique design, both m

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT COMPRISING THE SAME, AND ELECTRONIC DEVICE THEREOF

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Paragraph 0113; 0117-0118, (2018/05/17)

The present invention relates to a compound for an organic electric element, an organic electric element using the same, and an electronic device thereof. The organic electric element comprises: a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode. According to the present invention, the organic material layer includes the compound represented by the following formula 1, thereby lowering a driving voltage of the organic electric element and improving light emitting efficiency and life.COPYRIGHT KIPO 2018

Oxatriphyrins(2.1.1) incorporating an ortho-phenylene motif

Pawlicki,Garbicz,Szterenberg,Latos-Grazyski

supporting information, p. 1906 - 1909 (2015/02/19)

An understanding of fundamental aspects of archetypal organic structural motifs remains a key issue faced by the experimental and theoretical chemists. Two possible bonding modes for a disubstituted benzene ring, that is a meta and para, determines the p

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