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2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE is a heterocyclic chemical compound belonging to the class of imidazo[1,2-a]pyridines. It features a bromophenyl and a chloro group, both substituted on the imidazo[1,2-a]pyridine ring, and has shown potential pharmaceutical properties such as anti-inflammatory, antiviral, and antitumor activities.

96464-10-7

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96464-10-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE is used as a potential drug candidate for its anti-inflammatory, antiviral, and antitumor activities, making it a promising compound for the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE serves as a valuable building block in the synthesis of new chemical entities, contributing to the advancement of medicinal chemistry and the discovery of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 96464-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,6 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96464-10:
(7*9)+(6*6)+(5*4)+(4*6)+(3*4)+(2*1)+(1*0)=157
157 % 10 = 7
So 96464-10-7 is a valid CAS Registry Number.

96464-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names HMS590F11

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:96464-10-7 SDS

96464-10-7Relevant academic research and scientific papers

Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides

Singh, Bhagat,Ahmed, Jasimuddin,Biswas, Amit,Paira, Rupankar,Mandal, Swadhin K.

, p. 7242 - 7255 (2021/05/29)

Dehalogenative deuteration reactions are generally performed through metal-mediated processes. This report demonstrates a mild protocol for hydrodehalogenation and dehalogenative deuteration of aryl/heteroaryl halides (39 examples) using a reduced odd alternant hydrocarbon phenalenyl under transition metal-free conditions and has been employed successfully for the incorporation of deuterium in various biologically active compounds. The combined approach of experimental and theoretical studies revealed a single electron transfer-based mechanism.

Synthesis and antimicrobial activity of novel imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones

Rajitha,Ravibabu,Ramesh,Rajitha

, p. 1989 - 1998 (2016/03/16)

A novel series of imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones were synthesized via multistep synthesis starting from 2-aminopyridine on cyclisation with phenacyl bromide followed by Vilsmeier-Haack and Kn

Synthesis of bridgehead nitrogen heterocycles on a solid surface

Ponnala, Shashikanth,Kumar, S. T. V. S. Kiran,Bhat, Bashir A.,Sahu, Devi Prasad

, p. 901 - 906 (2007/10/03)

Bridgehead nitrogen heterocycles were synthesized from heteroaromatic amidines and cyclic or acyclic α-bromoketones under solvent-free conditions at room temperature on a solid surface in excellent yields, which are higher than those obtained with hithert

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