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1H-Indazole-1-carboxylic acid, 2,3-dihydro-3-oxo-2-(phenylmethyl)-, ethyl ester is a complex organic compound with the chemical formula C16H15NO3. It is a derivative of indazole, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyrazole ring. The molecule features a carboxylic acid group at the 1-position, a 2,3-dihydro-3-oxo structure, and a phenylmethyl group attached to the 2-position. The ethyl ester functional group is present, indicating that the carboxylic acid group is esterified with an ethyl group. 1H-Indazole-1-carboxylic acid, 2,3-dihydro-3-oxo-2-(phenylmethyl)-, ethyl ester is likely to be used in pharmaceutical or chemical research, potentially as an intermediate in the synthesis of various drugs or other organic compounds. Its specific applications and properties would depend on the context in which it is being studied or used.

1848-43-7

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1848-43-7 Usage

Type of compound

Organic compound

Derivative

Indazole

Contains groups

Carboxylic acid group, ethyl ester group, phenylmethyl group

Usage

Organic synthesis, pharmaceutical research

Potential properties

Pharmacological properties

Check Digit Verification of cas no

The CAS Registry Mumber 1848-43-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1848-43:
(6*1)+(5*8)+(4*4)+(3*8)+(2*4)+(1*3)=97
97 % 10 = 7
So 1848-43-7 is a valid CAS Registry Number.

1848-43-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-3-oxo-2,3-dihydro-indazole-1-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 1-Ethoxycarbonyl-2-benzyl-indazolon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1848-43-7 SDS

1848-43-7Relevant 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

Hypolipidemic Activity of Phthalimide Derivatives. 7. Structure-Activity Studies of Indazolone Analogues

Wyrick, Steven D.,Voorstad, P. Josee,Cocolas, George,Hall, Iris H.

, p. 768 - 772 (2007/10/02)

The apparent benefit of limiting serum cholesterol and triglyceride levels either by dietary restriction or drug therapy has prompted work in our laboratories toward development of a suitable antihyperlipidemic agent.We have demonstrated the antihyperlipi

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