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4-iodo-10,11-dihydro-5H-dibenzo[a,d]cycloheptan-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70911-04-5

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70911-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70911-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,1 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70911-04:
(7*7)+(6*0)+(5*9)+(4*1)+(3*1)+(2*0)+(1*4)=105
105 % 10 = 5
So 70911-04-5 is a valid CAS Registry Number.

70911-04-5Relevant academic research and scientific papers

Analogues of antidepressants - Synthesis of new 4-amine derivatives of 10,11-dihydro-5H-dibenzo[a,d]cycloheptane

Romeiro, Gilberto A.,Martins, Paulo Roberto C.

, p. 227 - 232 (2001)

In this paper the synthesis of six new 10,11-dihydro-5H-dibenzo[a,d]cycloheptane derivatives, analogues of antidepressants agents are reported. The preparation involved the initial introduction of the iodine atom in the positon 4 of the dibenzosuberone 3 to give the compound 4, which was then treated with different nuclcophilic reagents, to produce the compounds 5a to 5f.

Antidepressant-like profile of action of two 4-amine derivatives of 10,11-dihydro-5H-dibenzo [a,d] cycloheptane in mice evaluated in the forced swimming test

Duarte, Filipe Silveira,Codeco Martins, Paulo Roberto,Romeiro, Gilberto Alves,Monteiro De Lima, Thereza Christina

, p. 1645 - 1650 (2007)

This study investigated the antidepressant-like effect of 4-amine derivatives of 10,11-dihydro-5H-dibenzo-alkylamine-cycloheptane, 4-amine (3-N,N-dimethylpropylamine)-10,11-dihydro-5H-dibenzo[a,d]cycloheptane-5-one (ADDCH1) and 1,2,3,4,8,9-hexahydro-dibenzocyclohepta[4,4a,5-ef]1,4-diazepin (ADDCH2), in a validated experimental model of depression, the forced swimming test (FST) in mice. Female adult mice were sub-chronically (three doses in 24 h) or repeatedly (once a day for 10 days) treated with either of the compounds and evaluated in the FST. The sub-chronic treatment promoted a dose-dependent reduction in the immobility time in the FST with the doses of 50 mg/kg (ADDCH1) and 30 mg/kg (ADDCH2) ip being the most effective (33% and 37% of reduction, respectively). A similar profile of action was observed in the animals repeatedly treated with ADDCH1 50 mg/kg or ADDCH2 30 mg/kg ip (for 10 days) and there was no sign of motor impairment or locomotor activation as evaluated in the rota-rod and open-field tests, respectively. These findings suggest that these amine derivatives of the system dibenzocycloheptane have an antidepressant-like action which could be of clinical interest and, therefore, deserves further investigation. In addition, putative underlying mechanisms of action are discussed.

4-Thio derivatives of dibenzosuberone: Potential antidepressant compounds

Martins, Paulo R.C.,Romeiro, Gilberto A.,Ribeiro, Carlos M.R.

experimental part, p. 383 - 387 (2011/04/12)

This work describes the synthesis of a series of nine 4-thio dibenzosuberone derivatives (10,11-dihydro-5Hdibenzo[ a,d]cycloheptane-5-one derivatives). Ullmann's reaction was used to synthesize six 4-thio dibenzosuberone derivatives 10-15 from 4-iodo dibe

Synthesis of a new benzocycleheptaquinoline system

Romeiro, Gilberto A.,Martins, Paulo Roberto C.

, p. 493 - 498 (2007/10/03)

The new heterocyclic benzocycloheptaquinoline 8a was synthetized with 44% yield, starting with dibenzosuberone 3 in five steps. The linear isomer was totaly identified by IR, NMR 1H and 13C and MS, spectroscopic methods.

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