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897-15-4

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  • 11-(3-Dimethylaminopropylidene)-6,11-dihydrodibenzo(b,e)thiepine hydrochloride Manufacturer/High quality/Best price/In stock

    Cas No: 897-15-4

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897-15-4 Usage

Chemical Properties

White or faintly yellow, crystalline powder.

Uses

Different sources of media describe the Uses of 897-15-4 differently. You can refer to the following data:
1. Dothiepin Hydrochloride is a tricyclic antidepressant.
2. Monoamine reuptake inhibitor; tricyclic antidepressant

Drug interactions

Potentially hazardous interactions with other drugsAlcohol: increased sedative effect.Analgesics: increased risk of CNS toxicity with tramadol; possibly increased risk of side effects with nefopam; possibly increased sedative effects with opioids.Anti-arrhythmics: increased risk of ventricular arrhythmias with amiodarone - avoid; increased risk of ventricular arrhythmias with disopyramide, dronedarone, flecainide or propafenone - avoid with dronedarone.Antibacterials: increased risk of ventricular arrhythmias with moxifloxacin and possibly delamanid and telithromycin - avoid with moxifloxacin.Anticoagulants: may alter anticoagulant effect of coumarins.Antidepressants: enhanced CNS excitation and hypertension with MAOIs and moclobemide - avoid; concentration possibly increased with SSRIs; risk of ventricular arrhythmias with citalopram and escitalopram - avoid; possible increased risk of convulsions with vortioxetine.Antiepileptics: convulsive threshold lowered; concentration reduced by carbamazepine, phenobarbital and possibly fosphenytoin, phenytoin and primidone.Antimalarials: avoid with artemether/lumefantrine and piperaquine with artenimol.Antipsychotics: increased risk of ventricular arrhythmias especially with droperidol, fluphenazine, haloperidol, pimozide, risperidone, sulpiride and zuclopenthixol - avoid; increased antimuscarinic effects with clozapine and phenothiazines; concentration increased by antipsychoticsAntivirals: increased risk of ventricular arrhythmias with saquinavir - avoid; concentration possibly increased with ritonavir.Atomoxetine: increased risk of ventricular arrhythmias and possibly convulsions.Beta-blockers: increased risk of ventricular arrhythmias with sotalol.Clonidine: tricyclics antagonise hypotensive effect; increased risk of hypertension on clonidine withdrawal.Dapoxetine: possible increased risk of serotonergic effects - avoidDopaminergics: avoid use with entacapone; CNS toxicity reported with selegiline and rasagiline.

Metabolism

Dosulepin hydrochloride is readily absorbed from the gastrointestinal tract, and extensively demethylated by first-pass metabolism in the liver to its primary active metabolite, desmethyldothiepin (also termed northiaden). Paths of metabolism also include S-oxidation. Dosulepin is excreted in the urine, mainly in the form of its metabolites; small amounts are also excreted in the faeces. Elimination half-lives of about 14-24 and 23-46 hours have been reported for dosulepin and its metabolites, respectively. Dose in renal impairment GFR (mL/min) 20-50 Dose as in normal renal function. 10-20 Start with small dose and titrate according to response. <10 Start with small dose and titrate according to response. Dose in patients undergoing renal replacement therapies APD/CAPD Not dialysed. Dose as in GFR<10 mL/ min. HD Not dialysed. Dose as in GFR<10 mL/ min. HDF/High flux Unknown dialysability. Dose as in GFR<10 mL/min. CAV/VVHD Unknown dialysability. Dose as in GFR=10-20 mL/min. Important drug interactions Potentially hazardous interactions with other drugs Alcohol: increased sedative effect. Analgesics: increased risk of CNS toxicity with tramadol; possibly increased risk of side effects with nefopam; possibly increased sedative effects with opioids. Anti-arrhythmics: increased risk of ventricular arrhythmias with amiodarone - avoid; increased risk of ventricular arrhythmias with disopyramide, dronedarone, flecainide or propafenone - avoid with dronedarone. Antibacterials: increased risk of ventricular arrhythmias with moxifloxacin and possibly delamanid and telithromycin - avoid with moxifloxacin. Anticoagulants: may alter anticoagulant effect of coumarins. Antidepressants: enhanced CNS excitation and hypertension with MAOIs and moclobemide - avoid; concentration possibly increased with SSRIs; risk of ventricular arrhythmias with citalopram and escitalopram - avoid; possible increased risk of convulsions with vortioxetine. Antiepileptics: convulsive threshold lowered; concentration reduced by carbamazepine, phenobarbital and possibly fosphenytoin, phenytoin and primidone. Antimalarials: avoid with artemether/lumefantrine and piperaquine with

Check Digit Verification of cas no

The CAS Registry Mumber 897-15-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 897-15:
(5*8)+(4*9)+(3*7)+(2*1)+(1*5)=104
104 % 10 = 4
So 897-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NS.ClH/c1-20(2)13-7-11-17-16-9-4-3-8-15(16)14-21-19-12-6-5-10-18(17)19;/h3-6,8-12H,7,13-14H2,1-2H3;1H

897-15-4 Well-known Company Product Price

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  • (D2962000)  Dosulepin hydrochloride  European Pharmacopoeia (EP) Reference Standard

  • 897-15-4

  • D2962000

  • 1,880.19CNY

  • Detail

897-15-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dothiepin hydrochloride

1.2 Other means of identification

Product number -
Other names Dosulepinhydrochlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:897-15-4 SDS

897-15-4Synthetic route

dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In diethyl ether; ethanol
chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

11-<3-(Methyl-ethoxycarbonylamino)-propyliden>-6,11-dihydro-dibenzothiepin
2025-60-7

11-<3-(Methyl-ethoxycarbonylamino)-propyliden>-6,11-dihydro-dibenzothiepin

Conditions
ConditionsYield
With sodium hydrogencarbonate In toluene for 6h; Heating;92%
dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

N-methyldibenzothiepin-Δ11(6H),γ-propylamine
1154-09-2

N-methyldibenzothiepin-Δ11(6H),γ-propylamine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 92 percent / 1.) NaHCO3 / toluene / 6 h / Heating
2: 77 percent / KOH / butan-1-ol / 4 h / Heating
View Scheme
dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

3-thiepin-11-ylidene)propyl>-N-methylamino>propionic acid

3-thiepin-11-ylidene)propyl>-N-methylamino>propionic acid

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 92 percent / 1.) NaHCO3 / toluene / 6 h / Heating
2: 77 percent / KOH / butan-1-ol / 4 h / Heating
3: ethanol / 2 h / Heating
4: NaOH / methanol / 0.5 h / Heating
View Scheme
dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

3-(Methyl-{3-[11H-10-thia-dibenzo[a,d]cyclohepten-(5Z)-ylidene]-propyl}-amino)-propionic acid

3-(Methyl-{3-[11H-10-thia-dibenzo[a,d]cyclohepten-(5Z)-ylidene]-propyl}-amino)-propionic acid

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 92 percent / 1.) NaHCO3 / toluene / 6 h / Heating
2: 77 percent / KOH / butan-1-ol / 4 h / Heating
3: ethanol / 2 h / Heating
4: NaOH / methanol / 0.5 h / Heating
View Scheme
dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

ethyl 3-thiepin-11-ylidene)propyl>-N-methylamino>propionate

ethyl 3-thiepin-11-ylidene)propyl>-N-methylamino>propionate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 92 percent / 1.) NaHCO3 / toluene / 6 h / Heating
2: 77 percent / KOH / butan-1-ol / 4 h / Heating
3: ethanol / 2 h / Heating
View Scheme
dosulepin hydrochloride
897-15-4

dosulepin hydrochloride

3-(Methyl-{3-[11H-10-thia-dibenzo[a,d]cyclohepten-(5Z)-ylidene]-propyl}-amino)-propionic acid ethyl ester

3-(Methyl-{3-[11H-10-thia-dibenzo[a,d]cyclohepten-(5Z)-ylidene]-propyl}-amino)-propionic acid ethyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 92 percent / 1.) NaHCO3 / toluene / 6 h / Heating
2: 77 percent / KOH / butan-1-ol / 4 h / Heating
3: ethanol / 2 h / Heating
View Scheme

897-15-4Upstream product

897-15-4Relevant articles and documents

DOTHIEPIN AND METHODS OF USING THE SAME TO TREAT SLEEP DISORDERS

-

Page/Page column 20-21, (2010/11/29)

The invention relates to dothiepin, metabolites of dothiepin, isomers of the same, and pharmaceutically-acceptable salts and prodrugs of the same; compositions containing the same, and the use of any of the aforementioned for the treatment of sleep disorders.

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