| Weight | 295.451 g/mol |
|---|---|
| Formula | C19H21NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
113-53-1 (113-53-1)
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- The DDT story: ed. by Kenneth Mellanby. ISBN 0-948404-53-1 [113 pp; 22.50 (UK) 24.00 (overseas)]. Farnham, UK: British Crop Protection Council. 1992 (Crop Protection, 1994)
- Literature Review : OPTIMIZED DESIGN: CHARACTERISTIC VIBRATION SHAPES AND RESONATORS Brach, R. M. J. Acoust. Soc. Amer. 53 (1), 113-119 (Jan. 1973) 23 refs Refer to Abstract No. 73-528 (The Shock and Vibration Digest, 1973)
- Huserkampf in Dortmund, Teil 3: Aldinghoferstrae 16, Alter Mhlenweg 6, Bornstrae 206, Bornstrae 65, Borsigstrae 67, Dorstfelder Hellweg 15, Ernst-Mehlich-Strae, Gronaustrae 12, Kleine Kielstrae, Hermannstrae 46, Jacobstrae 1, Saarlandstrae 111-113, Schwarzer Rabe, Seydlitzstrae 14 und 18, Speicherstrae 51/53, Wrthstrae 1, 22 (24) und 58 (57) - Materialien zur Analyse von Opposition (2013)
- Migration and the Search for Home: Mapping Domestic Space in Migrants Everyday Lives, Paolo Boccagni. Palgrave Macmillan, New York (2017), xxi and 113 pp., 53,49 (Hardback), ISBN: 978-1-137-58801-2 (Emotion, Space and Society, 2017)
- The DDT story . By Kenneth Mellanby. (Surrey: British Crop Protection Council, 1992). 113 pp.Hard cover 22.50, overseas 27.00/$50.ISBN 0-948404-53-1 (Bulletin of Entomological Research, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN(C)CCC=C1C2=CC=CC=C2CSC3=CC=CC=C31
-
InChIKeyPHTUQLWOUWZIMZ-UHFFFAOYSA-N
- Pubchem - 113-53-1
- Wikipedia - dothiepin
Dosulepin, also known as dothiepin and sold under the brand name Prothiaden among others, is a tricyclic antidepressant (TCA) which is used in the treatment of depression. Dosulepin was once the most frequently prescribed antidepressant in the United Kingdom, but it is no longer widely used due to its relatively high toxicity in overdose without therapeutic advantages over other TCAs. It acts as a serotoninnorepinephrine reuptake inhibitor (SNRI) and also has other activities including antihistamine, antiadrenergic, antiserotonergic, anticholinergic, and sodium channel-blocking effects.
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