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115310-16-2

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115310-16-2 Usage

Structure

Benzene ring and indazole ring
The compound consists of a benzene ring, which is a six-membered ring with alternating single and double bonds, and an indazole ring, which is a five-membered ring containing two nitrogen atoms and one double bond.

Carbonyl group

Presence of C=O
The compound contains a carbonyl group (C=O), which is a functional group consisting of a carbon atom double-bonded to an oxygen atom.

Heterocyclic compound

Containing heteroatoms in the ring
The compound is classified as a heterocyclic compound because it contains nitrogen atoms (heteroatoms) in its ring structure, which differ from the carbon atoms in the ring.

Potential applications

Pharmaceutical and medicinal chemistry
1-benzyl-6,7-dihydro-1H-indazol-4(5H)-one has potential applications in the pharmaceutical and medicinal chemistry fields, as it can be used as a building block for the synthesis of other compounds.

Research value

Drug discovery and development
The compound's structure and properties make it a valuable tool for researchers and chemists working in drug discovery and development, as it can be used to create new compounds with potential therapeutic effects.

Biological activities and pharmacological properties

Target for further investigation
The potential biological activities and pharmacological properties of 1-benzyl-6,7-dihydro-1H-indazol-4(5H)-one make it a target for further investigation and development in the field of medicinal chemistry, as it may lead to the discovery of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 115310-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,1 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115310-16:
(8*1)+(7*1)+(6*5)+(5*3)+(4*1)+(3*0)+(2*1)+(1*6)=72
72 % 10 = 2
So 115310-16-2 is a valid CAS Registry Number.

115310-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-6,7-dihydro-5H-indazol-4-one

1.2 Other means of identification

Product number -
Other names 1-BENZYL-1,5,6,7-TETRAHYDRO-INDAZOL-4-ONE

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:115310-16-2 SDS

115310-16-2Relevant articles and documents

1,5,6,7-Tetrahydro-4H-indazol-4-ones as human neutrophil elastase (HNE) inhibitors

Bartolucci, Gianluca,Cantini, Niccolo,Crocetti, Letizia,Giovannoni, Maria Paola,Guerrini, Gabriella,Pallecchi, Marco,Quinn, Mark T.,Schepetkin, Igor A.,Teodori, Elisabetta,Vergelli, Claudia

supporting information, (2021/10/04)

Human neutrophil elastase (HNE) is a serine protease that is expressed in polymorphonuclear neutrophils. It has been recognized as an important therapeutic target for treating inflammatory diseases, especially related to the respiratory system, but also f

Pyrazolo[3,4-h]quinolines promising photosensitizing agents in the treatment of cancer

Spanò, Virginia,Parrino, Barbara,Carbone, Anna,Montalbano, Alessandra,Salvador, Alessia,Brun, Paola,Vedaldi, Daniela,Diana, Patrizia,Cirrincione, Girolamo,Barraja, Paola

, p. 334 - 351 (2015/09/01)

A new series of pyrazolo[3,4-h]quinolines, heteroanalogues of angelicin was conveniently prepared with a broad substitution pattern. A large number of derivatives was obtained and the cellular photocytotoxicity was evaluated in vitro against 5 different h

SYNTHESIS OF ANGULAR BENZODIPYRAZOLES AND RELATED SYSTEMS

Peet, Norton P.,LeTourneau, Michael E.

, p. 41 - 72 (2007/10/02)

A series of benzodipyrazoles was prepared from cyclohexane-1,3-dione.Several related systems with different central rings were also prepared.In addition, benzodipyrazoles were synthesized from 1,4-cyclohexanedione monoethylene

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