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(E)-3-(2-hydroxyphenyl)-1-(pyridin-4-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18455-65-7

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18455-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18455-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18455-65:
(7*1)+(6*8)+(5*4)+(4*5)+(3*5)+(2*6)+(1*5)=127
127 % 10 = 7
So 18455-65-7 is a valid CAS Registry Number.

18455-65-7Relevant academic research and scientific papers

Intramolecular oxidative coupling: I2/TBHP/NaN3-mediated synthesis of benzofuran derivatives

Xu, Wengang,Li, Qingcui,Cao, Chuanpeng,Zhang, Fanglin,Zheng, Hua

supporting information, p. 6158 - 6161 (2015/06/08)

A novel intramolecular oxidative coupling reaction has been established to prepare benzofuran derivatives via direct C(sp2)-H functionalization for the formation of C-O bond. This transformation is mediated by I2/TBHP/NaN3 under metal-free conditions and a catalytic amount of NaN3 plays a crucial role in the reaction. Furthermore, the reaction tolerates a broad substrate scope with average to excellent yields.

Hydroxypyridinechromene and pyridinechalcone: Two coupled photochrom systems

Leydet, Yoann,Jorge Parola,Pina, Fernando

experimental part, p. 545 - 555 (2010/05/18)

Substitution of the phenyl group in 2-hydroxychalcones by a 4-pyridine unit dramatically changes the network of chemical reactions of this compound: trans-chalcone-type(Ct), d.v-chalcone-type (Cc), and a hemiketal (hydroxy-4-pyridinechromene) (B) and their protonated forms are formed, but the presence of a flavylium-type cation could not be detected even at very acidic pH values. Moreover, whereas in 2-phenyl-2-benzopyryli urn compounds B and Cc are generally elusive species whose kinetic processes in aqueous solutions occur on the sub-second time-scale, in the present compound these species equilibrate on a timescale four orders of magnitude lower. Complete characterization of the equilibrium and kinetics of the reaction network could thus be achieved by 1H NMR spectros- copy and UV/Vis spectrophotometry. The network of chemical reactions exhibits cis-tmns photoisomerization, as well as photochromism between the hemiketal and the chalcone-type spe-cies. The irradiation of Ct in MeOH/ H2O (1:1) at 365 nm produces B almost quantitatively through two consecutive photochemical reactions: Ct→C c pho-toisomerization followed by Cc→ B photo ring closure with a global quan-tum yield of 0.02. On the other hand, irradiation of B at 254 nm leads to a photostationary state composed by 80% Ct and 20% B, with a quantum yield of 0.21.

New spiro-piperidines as 5-HT2B receptor antagonists

Bienayme, Hugues,Chene, Laurent,Grisoni, Serge,Grondin, Antonio,Kaloun, El-Bachir,Poigny, Stephane,Rahali, Houcine,Tam, Eric

, p. 4830 - 4833 (2007/10/03)

A functional screening highlighted a series of spiro-piperidines as 5-HT2B receptor antagonists. Preliminary structure-activity relationship has been explored driving to potent antagonists (IC50 = 1 nM) and indicating directions for

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