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1-[(phenyl)carbonyl] 4-(naphthyl)semicarbazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18248-54-9

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18248-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18248-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18248-54:
(7*1)+(6*8)+(5*2)+(4*4)+(3*8)+(2*5)+(1*4)=119
119 % 10 = 9
So 18248-54-9 is a valid CAS Registry Number.

18248-54-9Relevant academic research and scientific papers

Synthesis, characterization and antioxidant activities of semicarbazide and thiosemicarbazide derivatives

Alam, Faima,Ali, Basharat,Ali, Mahboob,Khan, Khalid Mohammed,Khan, Momin,Manaf, Abdul,Zaman, Khair

, p. 475 - 483 (2021/08/21)

In this research work Semicarbazide, thiosemicarbazide derivatives 3 to 25 were synthesized by conventional methods with high percentage yield and reaction rate. 1H-NMR and EIMS spectroscopic techniques were used to elucidate the structure of t

Discovery and SAR of a series of agonists at orphan G protein-coupled receptor 139

Shi, Feng,Shen, Jing Kang,Chen, Danqi,Fog, Karina,Thirstrup, Kenneth,Hentzer, Morten,Karlsson, Jens-Jakob,Menon, Veena,Jones, Kenneth A.,Smith, Kelli E.,Smith, Garrick

scheme or table, p. 303 - 306 (2011/06/21)

GPR139 is an orphan G-protein coupled receptor (GPCR) which is primarily expressed in the central nervous system (CNS). In order to explore the biological function of this receptor, selective tool compounds are required. A screening campaign identified compound 1a as a high potency GPR139 agonist with an EC50 = 39 nM in a calcium mobilization assay in CHO-K1 cells stably expressing the GPR139 receptor. In the absence of a known endogenous ligand, the maximum effect was set as 100% for 1a. Screening against 90 diverse targets revealed no cross-reactivity issues. Assessment of the pharmacokinetic properties showed limited utility as in vivo tool compound in rat with a poor whole brain exposure of 61 ng/g and a brain/plasma (b/p) ratio of 0.03. Attempts to identify a more suitable analogue identified the des-nitrogen analogue 1s with a reduced polar surface area of 76.7 A2 and an improved b/p ratio of 2.8. The whole brain exposure remained low at 95 ng/g due to a low plasma exposure.

An efficient synthesis of 1,3,4-oxadiazoles from N,N′-diacylhydrazines using Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts as condensing agents

Mazurkiewicz,Grymel

, p. 77 - 82 (2007/10/03)

1,3,4-Oxadiazoles including 2-amino derivatives were effectively synthesized by treatment of N,N′-diacylhydrazines or N-acylsemicarbazides with Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts in the presence of Et3N in CH2Cl2 under mild conditions.

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