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2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride

  • Name 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride
  • CAS 4335-29-9
  • Purity 99%
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What is the 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride ?

2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is , while it's Molecular Formula is C11H10N2S. Used in Pharmaceutical Industry:
2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is used as a ligand for certain receptors in the pharmaceutical industry for its potential as a therapeutic agent for neurological disorders. Its biological activity and receptor binding properties make it a promising candidate for the development of new drugs to treat various neurological conditions.
Used in Neuroscience Research:
In the field of neuroscience, 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is used as a research tool to study the mechanisms of action and potential therapeutic effects of imidazothiazole derivatives on neurological disorders. Its investigation helps researchers understand the role of specific receptors and pathways in these conditions, guiding the development of more effective treatments.

What is the CAS number for 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride ?

The CAS number of 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is 4335-29-9.

More information of 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride 4335-29-9 are:

Synonyms

2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride;

CAS?Number

4335-29-9

Molecular Formula

C11H10N2S

Molecular Weight

202.2755

Density

1.31g/cm3

Boiling Point

421.5°Cat760mmHg

Flash Point

208.7°C

HS CODE

2934100090

PSA

43.12000

LogP

3.45780

What is 2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride (4335-29-9) used for?

2,3-dihydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is a chemical compound with the molecular formula C11H10N2S?HCl. It is a derivative of imidazothiazole, a heterocyclic compound consisting of an imidazole ring fused to a thiazole ring. This specific compound features a phenyl group attached to the imidazothiazole core, and it is a monohydrochloride salt, indicating the presence of a hydrogen chloride molecule. It is often used in pharmaceutical applications, particularly as an intermediate in the synthesis of various drugs. The compound is known for its potential biological activities, such as anti-inflammatory and analgesic properties, and is a subject of interest in medicinal chemistry research.

InChI:InChI=1/C11H10N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,8H,6-7H2;1H

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