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CAS No.: | 68-91-7 |
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Name: | trimetaphan camsilate |
Molecular Structure: | |
Formula: | C22H25N2OS•C10H15O4S |
Molecular Weight: | 596.812 |
Synonyms: | trimetaphan camsilate;Trimetaphan camsylate;TRIMETHAPHANCAMPHORSULPHONATE;Trimethaphan camphorsulfonate |
Melting Point: | 245 °C (decomp) |
Safety: | Poison by ingestion, intraperitoneal, intravenous, and intramuscular routes. Moderately toxic by subcutaneous route. Experimental reproductive effects. When heated to decomposition it emits very toxic fumes of NOx and SOx. |
PSA: | 131.50000 |
LogP: | 5.53950 |
IUPAC Name: Trimetaphan camsilate
Molecular Formula: C22H25N2OS•C10H15O4S
Molecular Weight: 596.86
Melting Point: 245 °C
Freely Rotating Bonds: 4
Polar Surface Area: 23.55 Å2
The Cas Register Number of Trimethiophane is 68-91-7.The chemical synonyms of Trimethiophane (CAS NO.68-91-7) are 1,3-Dibenzyl-2-oxodecahydrothieno[1',2':1,2]thieno[3,4-d]imidazol-5-ium (7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)methanesulfonate ; 2-Oxo-1,3-bis(phenylmethyl)decahydrothieno[1',2':1,2]thieno[3,4-d]imidazol-5-ium (7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)methanesulfonate ; Decahydro-2-oxo-1,3-bis(phenylmethyl)thieno[1',2':1,2]thieno[3,4-d]imidazol-5-ium salt with (1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid (1:1) ; Methioplegium ; Trimetaphan camphorsulfonate ; (7,7-Dimethyl-2-oxo-bicyclo[2.2.1]hept-1-yl)-methanesulfonate1,3-dibenzyl-2-oxo-decahydro-6a-thionia-1,3-diaza-cyclopenta[a]pentalene ; (7,7-Dimethyl-2-oxo-bicyclo[2.2.1]hept-1-yl)-methanesulfonate1,3-dibenzyl-2-oxo-decahydro-6a-thionia-1,3-diaza-cyclopenta[a]pentalene .The molecular structure of Trimethiophane (CAS NO.68-91-7) is.
Trimethiophane (CAS NO.68-91-7) is used as antihypertensive and ganglion blocking agent.
1. | orl-rat LD50:2494 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),528. | ||
2. | ipr-rat LD50:141 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),528. | ||
3. | scu-rat LD50:2024 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),528. | ||
4. | ivn-rat LD50:21 mg/kg CLDND* | |||
5. | orl-mus LD50:927 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),528. | ||
6. | ipr-mus LD50:112 mg/kg | FAATDF Fundamental and Applied Toxicology. 6 (1986),35. | ||
7. | scu-mus LD50:629 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),528. | ||
8. | ivn-mus LD50:14,400 µg/kg | RPTOAN Russian Pharmacology and Toxicology. Translation of FATOAO. 37 (1974),7. | ||
9. | ims-mus LD50:133 mg/kg | YKYUA6 Yakkyoku. Pharmacy. 28 (1977),495. | ||
10. | o |
Poison by ingestion, intraperitoneal, intravenous, and intramuscular routes. Moderately toxic by subcutaneous route. Experimental reproductive effects. When heated to decomposition it emits very toxic fumes of NOx and SOx.