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1018814-40-8

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1018814-40-8 Usage

General Description

7-Bromo-2-phenylimidazo[1,2-a]pyridine is a chemical compound with the molecular formula C11H8BrN3. It is a heterocyclic compound that contains a bromine atom and a phenyl group attached to an imidazo[1,2-a]pyridine ring system. 7-Bromo-2-phenylimidazo[1,2-a]pyridine is commonly used in organic synthesis and pharmaceutical research as a building block for the development of new drugs and bioactive molecules. It may also have potential applications in the field of medicinal chemistry due to its unique structural properties and potential biological activities. Additionally, it is important to handle and store this chemical with caution, as it may pose health and safety risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 1018814-40-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,8,1 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1018814-40:
(9*1)+(8*0)+(7*1)+(6*8)+(5*8)+(4*1)+(3*4)+(2*4)+(1*0)=128
128 % 10 = 8
So 1018814-40-8 is a valid CAS Registry Number.

1018814-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromo-2-phenylimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:1018814-40-8 SDS

1018814-40-8Relevant articles and documents

Metal-Free Regioselective Alkylation of Imidazo[1,2- a ]pyridines with N -Hydroxyphthalimide Esters under Organic Photoredox Catalysis

Jin, Can,Sun, Bin,Xu, Min,Xu, Tengwei,Yang, Jin,Zhang, Liang,Zhu, Rui

, p. 363 - 368 (2020)

A visible-light-induced direct C-H alkylation of imidazo[1,2- a ]pyridines has been developed. It proceeds at room temperature by employing inexpensive Eosin Y as a photocatalyst and alkyl N -hydroxyphthalimide (NHP) esters as alkylation reagents. A varie

Palladium-Catalyzed C-N Coupling of Pyrazole Amides with Triazolo- And Imidazopyridine Bromides in Ethanol

Bliss, Fritz,Fantasia, Serena,Le Coz, Erwann,Püntener, Kurt

supporting information, p. 457 - 468 (2021/02/01)

An efficient palladium-catalyzed coupling between a pyrazole amide and a heteroaryl bromide was developed to enable the streamlined synthesis of a lead candidate for schizophrenia treatment. Process robustness and scalability were achieved using ethanol a

Imidazo[1,2- a]pyridine derivatives as aldehyde dehydrogenase inhibitors: Novel chemotypes to target glioblastoma stem cells

Quattrini, Luca,Gelardi, Edoardo Luigi Maria,Coviello, Vito,Sartini, Stefania,Ferraris, Davide Maria,Mori, Mattia,Nakano, Ichiro,Garavaglia, Silvia,La Motta, Concettina

, p. 4603 - 4616 (2020/06/08)

Glioblastoma multiforme (GBM) is the deadliest form of brain tumor. It is known for its ability to escape the therapeutic options available to date thanks to the presence of a subset of cells endowed with stem-like properties and ability to resist to cyto

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