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3-Benzyloxy-1H-indazole is a chemical compound with the molecular formula C15H12N2O. It is a derivative of indazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrazole ring. The "3-benzyloxy" part of the name indicates that a benzyloxy group (C6H5CH2O-) is attached to the third carbon of the indazole ring. 3-benzyloxy-1H-indazole is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and potential reactivity. It is typically synthesized through various chemical reactions, such as the condensation of indazole with benzyl alcohol in the presence of a catalyst. The compound is a white to off-white solid and is soluble in organic solvents. Its applications span across various industries, including the development of new drugs and the creation of novel chemical compounds for research purposes.

1848-47-1

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1848-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1848-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1848-47:
(6*1)+(5*8)+(4*4)+(3*8)+(2*4)+(1*7)=101
101 % 10 = 1
So 1848-47-1 is a valid CAS Registry Number.

1848-47-1Downstream Products

1848-47-1Relevant academic research and scientific papers

Synthesis, biological evaluation and chemometric analysis of indazole derivatives. 1,2-Disubstituted 5-nitroindazolinones, new prototypes of antichagasic drug

Vega, María Celeste,Rolón, Miriam,Montero-Torres, Alina,Fonseca-Berzal, Cristina,Escario, José Antonio,Gómez-Barrio, Alicia,Gálvez, Jorge,Marrero-Ponce, Yovani,Arán, Vicente J.

supporting information, p. 214 - 227 (2013/02/23)

Chagas disease chemotherapy, currently based on only two drugs, nifurtimox and benznidazole, is far from satisfactory and therefore the development of new antichagasic compounds remains an important goal. On the basis of antichagasic properties previously

Study of 5-nitroindazoles' anti-Trypanosoma cruzi mode of action: Electrochemical behaviour and ESR spectroscopic studies

Rodriguez, Jorge,Gerpe, Alejandra,Aguirre, Gabriela,Kemmerling, Ulrike,Piro, Oscar E.,Aran, Vicente J.,Maya, Juan Diego,Olea-Azar, Claudio,Gonzalez, Mercedes,Cerecetto, Hugo

scheme or table, p. 1545 - 1553 (2009/07/04)

New indazole derivatives have been developed to know about structural requirements for adequate anti-Trypanosoma cruzi activity. In relation to position 1 of indazole ring, we have observed that a butylaminopentyl substituent (14) affords good activity, b

Indazolinones, a new series of redox-active 5-lipoxygenase inhibitors with built-in selectivity and oral activity

Bruneau,Delvare,Edwards,McMillan

, p. 1028 - 1036 (2007/10/02)

Since the hypothetical mechanisms of hydroperoxydation of arachidonic acid by, respectively, 5-lipoxygenase (5-LPO) and cyclooxygenase (CO) involve a redox cycle, a compound which reduces 5-LPO and CO to their inactive state would give a nonselective inhi

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