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6-Dipropylamino-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-ol; hydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76413-86-0

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76413-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76413-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,1 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76413-86:
(7*7)+(6*6)+(5*4)+(4*1)+(3*3)+(2*8)+(1*6)=140
140 % 10 = 0
So 76413-86-0 is a valid CAS Registry Number.

76413-86-0Downstream Products

76413-86-0Relevant academic research and scientific papers

Monophenolic 2-(dipropylamino)indans and related compounds: Central dopamine-receptor stimulating activity

Hacksell,Arvidsson,Svensson,Nilsson,Wikstroem,Lindberg,Sanchez,Hjorth,Carlsson,Paalzow

, p. 429 - 434 (1981)

Monophenolic 2-(dipropylamino)indans and related compounds have been synthesized and tested for central dopamine-receptor stimulating activity, using biochemical and behavioral tests in rats and emesis tests in dogs. The active compounds possess similar relative potencies in eliciting the three different dopamine-receptor mediated effects measured. 4-Hydroxy-2-(dipropylamino)indan was the most potent of the new compounds. The corresponding 5-hydroxy analogue was less active. 4-Hydroxy-2-[(dipropylamino)methyl]indan is a new type of dopaminergic agent with a phenylpropylamine moiety in its framework instead of the phenylethylamine structure, common to most dopamine-receptor agonists. This compound was 10-20 times less active than apomorphine. 6,7,8,9-Tetrahydro-1-hydroxy-N,N-dipropyl-5H-6-benzocycloheptenylamine-5-hydroxy-2-[(dipropylamino)methyl]tetralin were both inactive. Since the intramolecular distances between functional groups in the indans studied here are different from those in, for example, apomorphine, it is concluded that a certain variation of these distances can be accepted by the receptor. It could also be demonstrated that the position of the OH group on the aromatic ring is of importance for the activity and that emetic activity may be associated with dopaminergic agonists of the indan as well as of the tetralin type of structure.

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