Isothipendyl structure
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Common Name | Isothipendyl | ||
|---|---|---|---|---|
| CAS Number | 482-15-5 | Molecular Weight | 285.40700 | |
| Density | 1.167g/cm3 | Boiling Point | 421.3ºC at 760mmHg | |
| Molecular Formula | C16H19N3S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 208.6ºC | |
Use of IsothipendylIsothipendyl (AY 56012), an azaphenothiazine derivative, is a potent histamine 1 (H1) receptor antagonist. Isothipendyl is a primary metabolite[1]. |
| Name | N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine |
|---|---|
| Synonym | More Synonyms |
| Description | Isothipendyl (AY 56012), an azaphenothiazine derivative, is a potent histamine 1 (H1) receptor antagonist. Isothipendyl is a primary metabolite[1]. |
|---|---|
| Related Catalog | |
| Target |
Human Endogenous Metabolite |
| Density | 1.167g/cm3 |
|---|---|
| Boiling Point | 421.3ºC at 760mmHg |
| Molecular Formula | C16H19N3S |
| Molecular Weight | 285.40700 |
| Flash Point | 208.6ºC |
| Exact Mass | 285.13000 |
| PSA | 44.67000 |
| LogP | 3.69940 |
| Vapour Pressure | 2.63E-07mmHg at 25°C |
| Index of Refraction | 1.62 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Isothipendyl CAS#:482-15-5 |
| Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
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Isothipendyl CAS#:482-15-5 |
| Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
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~%
Isothipendyl CAS#:482-15-5 |
| Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
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~%
Isothipendyl CAS#:482-15-5 |
| Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
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~%
Isothipendyl CAS#:482-15-5 |
| Literature: Yale; Sowinski Journal of the American Chemical Society, 1958 , vol. 80, p. 1651,1653 |
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~%
Isothipendyl CAS#:482-15-5 |
| Literature: Schuler,W.A.; Klebe,H. Justus Liebigs Annalen der Chemie, 1962 , vol. 653, p. 172 - 180 |
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Isothipendyl CAS#:482-15-5 |
| Literature: Schuler,W.A.; Klebe,H. Justus Liebigs Annalen der Chemie, 1962 , vol. 653, p. 172 - 180 |
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