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1-Benzyl-4-chloro-5-azaindole is a heterocyclic organic compound characterized by the molecular formula C14H11ClN2. It features a benzyl group and a chlorine atom attached to a five-membered nitrogen-containing ring, making it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. 1-Benzyl-4-chloro-5-azaindole has garnered interest due to its potential biological activities, such as antiviral and antitumor properties, as well as its utility as a fluorescent probe in various analytical and biological applications.

35636-10-3

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35636-10-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-Benzyl-4-chloro-5-azaindole serves as a key building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and functional groups contribute to the development of new molecules with therapeutic and pesticidal properties.
Used in Antiviral Applications:
1-Benzyl-4-chloro-5-azaindole is studied for its antiviral properties, potentially inhibiting the replication and infectivity of viruses, making it a candidate for the development of antiviral drugs.
Used in Antitumor Applications:
1-Benzyl-4-chloro-5-azaindole has been investigated for its antitumor properties, showing promise in inhibiting the growth and proliferation of cancer cells, thus contributing to the development of novel anticancer agents.
Used in Analytical and Biological Research:
1-Benzyl-4-chloro-5-azaindole's potential as a fluorescent probe makes it valuable in analytical and biological research. Its fluorescence properties can be utilized for detecting and monitoring various biological processes and interactions, enhancing the understanding of complex biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 35636-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35636-10:
(7*3)+(6*5)+(5*6)+(4*3)+(3*6)+(2*1)+(1*0)=113
113 % 10 = 3
So 35636-10-3 is a valid CAS Registry Number.

35636-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-chloropyrrolo[3,2-c]pyridine

1.2 Other means of identification

Product number -
Other names benzyl-1 chloro-4 pyrrolo<3,2-c>pyridine

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:35636-10-3 SDS

35636-10-3Relevant academic research and scientific papers

Structure-Based Design and Optimization of FPPQ, a Dual-Acting 5-HT3and 5-HT6Receptor Antagonist with Antipsychotic and Procognitive Properties

Zajdel, Pawe?,Grychowska, Katarzyna,Mogilski, Szczepan,Kurczab, Rafa?,Sata?a, Grzegorz,Bugno, Ryszard,Kos, Tomasz,Go?e?biowska, Joanna,Malikowska-Racia, Natalia,Nikiforuk, Agnieszka,Chaumont-Dubel, Séverine,Bantreil, Xavier,Paw?owski, Maciej,Martinez, Jean,Subra, Gilles,Lamaty, Frédéric,Marin, Philippe,Bojarski, Andrzej J.,Popik, Piotr

supporting information, p. 13279 - 13298 (2021/09/20)

In line with recent clinical trials demonstrating that ondansetron, a 5-HT3receptor (5-HT3R) antagonist, ameliorates cognitive deficits of schizophrenia and the known procognitive effects of 5-HT6receptor (5-HT6R) antagonists, we applied the hybridization strategy to design dual-acting 5-HT3/5-HT6R antagonists. We identified the first-in-class compoundFPPQ, which behaves as a 5-HT3R antagonist and a neutral antagonist 5-HT6R of the Gs pathway.FPPQshows selectivity over 87 targets and decent brain penetration. Likewise,FPPQinhibits phencyclidine (PCP)-induced hyperactivity and displays procognitive properties in the novel object recognition task. In contrast toFPPQ, neither 5-HT6R inverse agonist SB399885 nor neutral 5-HT6R antagonist CPPQ reversed (PCP)-induced hyperactivity. Thus, combination of 5-HT3R antagonism and 5-HT6R antagonism, exemplified byFPPQ, contributes to alleviating the positive-like symptoms. Present findings reveal critical structural features useful in a rational polypharmacological approach to target 5-HT3/5-HT6receptors and encourage further studies on dual-acting 5-HT3/5-HT6R antagonists for the treatment of psychiatric disorders.

NEW COMPOUNDS USEFUL FOR THE TREATMENT OF OBESITY, TYPE II DIABETES AND CNS DISORDERS

-

, (2008/06/13)

The present invention relates to compounds of the general formula (I), wherein P is sulfone or sulfonamide; and A, B, W, X, Y and R3 are as defined in the description;to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the prophylaxis and treatment of medical conditions relating to obesity, type II diabetes, and/or CNS disorders, to achieve reduction of body weight and of body weight gain.

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