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17954-81-3

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17954-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17954-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,5 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17954-81:
(7*1)+(6*7)+(5*9)+(4*5)+(3*4)+(2*8)+(1*1)=143
143 % 10 = 3
So 17954-81-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO2/c11-6-1-7-13-10-4-2-9(8-12)3-5-10/h2-5,8H,1,6-7H2

17954-81-3Relevant articles and documents

Design, synthesis, in silico analysis with PPAR-γ receptor and study of non-covalent interactions in unsymmetrical heterocyclic/phenyl fleximer

Singh, Ved Prakash,Dowarah, Jayanta,Marak, Brilliant N.,Tewari, Ashish Kumar

, p. 150 - 158 (2021)

This work deals with the design, synthesis, in silico analysis, crystallization, and the interpretation 2-cyano-3-{4-[2-(phthalimid-nyl)-propoxy]-phenyl}-acrylic acid ethyl ester (7). Analog 7 is designed based on rosiglitazone. The quantitative analysis

Bimodal detection of carbon dioxide using fluorescent molecular aggregates

Mishra, Rakesh K.,Vijayakumar, Samiyappan,Mal, Arindam,Karunakaran, Varsha,Janardhanan, Jith C.,Maiti, Kaustabh Kumar,Praveen, Vakayil K.,Ajayaghosh, Ayyappanpillai

, p. 6046 - 6049 (2019)

Cyano-substituted p-phenylenevinylene (R-1) aggregates exhibiting fluorescence and Raman spectroscopic responses towards CO2 are described. The aggregation-induced emission (AIE) as well as the aggregation-enhanced Raman scattering (AERS) of R-

Synthesis, Characterization and Biological Evaluation of Novel Triazole Linked Chromone Biheterocycle Analogs

Kalyani, Gade,Reddy, D. Ravisankar,Soujanya, Jilla

, p. 53 - 59 (2022/01/06)

The current work focused on the synthesis of novel chromone biheterocycle analogs followed by its characterization through physicochemical and spectral techniques like FTIR, mass and NMR spectroscopy. The basic triazole heterocycle and its analogs have di

A dual-acting 5-HT6 receptor inverse agonist/MAO-B inhibitor displays glioprotective and pro-cognitive properties

Canale, Vittorio,Grychowska, Katarzyna,Kurczab, Rafa?,Ryng, Mateusz,Keeri, Abdul Raheem,Sata?a, Grzegorz,Olejarz-Maciej, Agnieszka,Koczurkiewicz, Paulina,Drop, Marcin,Blicharz, Klaudia,Piska, Kamil,P?kala, El?bieta,Janiszewska, Paulina,Krawczyk, Martyna,Walczak, Maria,Chaumont-Dubel, Severine,Bojarski, Andrzej J.,Marin, Philippe,Popik, Piotr,Zajdel, Pawe?

supporting information, (2020/09/21)

The complex etiology of Alzheimer's disease has initiated a quest for multi-target ligands to address the multifactorial causes of this neurodegenerative disorder. In this context, we designed dual-acting 5-HT6 receptor (5-HT6R) anta

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