CL 218872 structure
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Common Name | CL 218872 | ||
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| CAS Number | 66548-69-4 | Molecular Weight | 278.23300 | |
| Density | 1.43g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C13H9F3N4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of CL 218872CL 218872 is a selective and orally active benzodiazepine of α1 subunit-containing GABAAreceptor with a Ki of 130 nM. CL 218872 exerts anxiolytic and anticonvulsant in vivo[1]. |
| Name | 3-methyl-6-[3-(trifluoromethyl)phenyl]-[1,2,4]triazolo[4,3-b]pyridazine |
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| Synonym | More Synonyms |
| Description | CL 218872 is a selective and orally active benzodiazepine of α1 subunit-containing GABAAreceptor with a Ki of 130 nM. CL 218872 exerts anxiolytic and anticonvulsant in vivo[1]. |
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| Related Catalog | |
| References |
| Density | 1.43g/cm3 |
|---|---|
| Molecular Formula | C13H9F3N4 |
| Molecular Weight | 278.23300 |
| Exact Mass | 278.07800 |
| PSA | 43.08000 |
| LogP | 3.11850 |
| Index of Refraction | 1.615 |
| Storage condition | -20°C |
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CL 218872 CAS#:66548-69-4 |
| Literature: American Cyanamid Company Patent: US4112095 A1, 1978 ; |
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CL 218872 CAS#:66548-69-4 |
| Literature: Lieberman, Daniel F.; Albright, J. Donald Journal of Heterocyclic Chemistry, 1988 , vol. 25, p. 827 - 830 |
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CL 218872 CAS#:66548-69-4 |
| Literature: Albright, J. D.; Moran, D. B.; Wright, W. B.; Collins, J. B.; Beer, B.; et al. Journal of Medicinal Chemistry, 1981 , vol. 24, # 5 p. 592 - 600 |
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CL 218872 CAS#:66548-69-4 |
| Literature: Lieberman, Daniel F.; Albright, J. Donald Journal of Heterocyclic Chemistry, 1988 , vol. 25, p. 827 - 830 |
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CL 218872 CAS#:66548-69-4 |
| Literature: Lieberman, Daniel F.; Albright, J. Donald Journal of Heterocyclic Chemistry, 1988 , vol. 25, p. 827 - 830 |
| CL 218,872 |
| Tocris-1709 |