39478-90-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is a derivative of 1,2-naphtalenediol, which means it has undergone a hydrogenation reaction, resulting in the addition of hydrogen atoms to the molecule.
Explanation
The compound contains a dimethylamino (-N(CH3)2) functional group attached to the 6th carbon atom of the naphthalene ring.
4. Crystalline solid
Explanation
The compound forms a solid with a well-defined, ordered crystal structure.
5. Potential biological activity
Explanation
Studies suggest that the compound may have biological effects, which could be useful in pharmaceutical applications.
6. Pharmaceutical and chemical industries
Explanation
The compound has been studied for its potential applications in these industries, indicating its potential use in drug development or chemical synthesis.
7. Organic synthesis
Explanation
The compound may be used as a building block or intermediate in the synthesis of other organic compounds.
8. Building block for new compounds
Explanation
Its structure and functional groups make it a potential starting point for the development of new chemical entities.
9. Further research required
Explanation
More studies are needed to fully understand the properties, potential uses, and safety of the compound in various applications.
Tetrahydro derivative
1,2-Naphthalenediol
Dimethylamino group
at the 6-position
Check Digit Verification of cas no
The CAS Registry Mumber 39478-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,4,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39478-90:
(7*3)+(6*9)+(5*4)+(4*7)+(3*8)+(2*9)+(1*0)=165
165 % 10 = 5
So 39478-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2.BrH/c1-13(2)9-4-5-10-8(7-9)3-6-11(14)12(10)15;/h3,6,9,14-15H,4-5,7H2,1-2H3;1H
39478-90-5Relevant academic research and scientific papers
Synthesis and pharmacology of some 2 aminotetralins. Dopamine receptor agonists
McDermed,McKenzie,Phillips
, p. 362 - 367 (2007/10/05)
A series of 2 amino 1,2,3,4 tetrahydronaphthalene compounds bearing substituents on the nitrogen and in the aromatic ring was synthesized from β tetralone intermediates. Compounds were screened in vivo for dopaminergic activity using tests in which apomorphine was especially active. It was found that apparent dopaminergic activity is inherent in 2 dialkylaminotetralins, the dipropylamine substitution being the most consistently productive amine group studied. Activity was greatly enhanced by proper substitution in the aromatic ring. The 5,6 dihydroxy group was the best potentiating group found. These data support the idea that the extended conformation for the phenylethylamine moiety of apomorphine and dopamine is favorable for dopaminergic agonist activity. They also suggest that an unetherified catechol group may not be essential for such activity.
