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6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE is a complex heterocyclic chemical compound that features a derivative structure of both thiazole and imidazole, with the addition of a phenyl group. 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE is recognized for its potential biological activities and pharmacological properties, which make it a valuable asset in pharmaceutical and biochemical research. Its distinctive structural composition allows for its application in the development of innovative drugs and chemical entities, as well as in the broader realms of organic synthesis, medicinal chemistry, and drug discovery.

75224-64-5

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75224-64-5 Usage

Uses

Used in Pharmaceutical and Biochemical Research:
6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE serves as a key component in the development of new pharmaceutical agents due to its inherent biological activities and pharmacological properties. It is utilized for its potential to contribute to the creation of novel drug candidates.
Used in Organic Synthesis:
In the field of organic synthesis, 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE is employed as a building block or intermediate in the synthesis of more complex organic compounds, leveraging its unique structural features to form new chemical entities.
Used in Medicinal Chemistry:
6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE is applied as a versatile molecule in medicinal chemistry for the design and modification of pharmaceutical compounds, taking advantage of its heterocyclic nature to enhance drug-like properties.
Used in Drug Discovery:
6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE plays a role in drug discovery processes, where its potential biological activities are explored and harnessed to identify new therapeutic agents, particularly those targeting specific diseases or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 75224-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,2 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75224-64:
(7*7)+(6*5)+(5*2)+(4*2)+(3*4)+(2*6)+(1*4)=125
125 % 10 = 5
So 75224-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2OS/c15-8-10-11(9-4-2-1-3-5-9)13-12-14(10)6-7-16-12/h1-5,8H,6-7H2

75224-64-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H50482)  2,3-Dihydro-6-phenylimidazo[2,1-b]thiazole-5-carboxaldehyde, 97%   

  • 75224-64-5

  • 1g

  • 1112.0CNY

  • Detail
  • Alfa Aesar

  • (H50482)  2,3-Dihydro-6-phenylimidazo[2,1-b]thiazole-5-carboxaldehyde, 97%   

  • 75224-64-5

  • 5g

  • 5017.0CNY

  • Detail

75224-64-5SDS

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 2,3-Dihydro-6-Phenylimidazo[2,1-b]Thiazole-5-Carboxaldehyde

1.2 Other means of identification

Product number -
Other names 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE

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:75224-64-5 SDS

75224-64-5Relevant academic research and scientific papers

Investigation on the effects of antimicrobial imidazo[2,1-b]Thiazole derivatives on the genitourinary microflora

Morigi, Rita,Vitali, Beatrice,Prata, Cecilia,Palomino, Rogers A. ?.,Graziadio, Alessandra,Locatelli, Alessandra,Rambald, Mirella,Leoni, Alberto

, p. 311 - 319 (2018/05/17)

Background: Fused five-membered heterocyclic rings containing bridgehead nitrogen atom are particularly versatile in the field of medicinal chemistry because of their different biological activities. Among them, the imidazo[2,1-b]thiazole is an attractive

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