CAS 59709-57-8
:6,7-Dihydroxy-1-methyl-1,2,3,4-tetrahydroisoquinoline hydrobromide
Description:
6,7-Dihydroxy-1-methyl-1,2,3,4-tetrahydroisoquinoline hydrobromide is a chemical compound that belongs to the class of tetrahydroisoquinolines, which are bicyclic organic compounds. This substance features a tetrahydroisoquinoline core with two hydroxyl (-OH) groups at the 6 and 7 positions, and a methyl group at the 1 position, contributing to its unique properties. The hydrobromide salt form indicates that it is combined with hydrobromic acid, enhancing its solubility in water and making it suitable for various applications, particularly in biological and pharmaceutical contexts. The presence of hydroxyl groups suggests potential for hydrogen bonding, which can influence its reactivity and interactions with biological molecules. This compound may exhibit various pharmacological activities, although specific biological effects would depend on further research. As with many organic compounds, safety and handling precautions should be observed, particularly due to its classification and potential biological effects.
Formula:C10H14NO2
InChI:InChI=1/C10H13NO2/c1-6-8-5-10(13)9(12)4-7(8)2-3-11-6/h4-6,11-13H,2-3H2,1H3/p+1/t6-/m1/s1
Synonyms:- 1,2,3,4-Tetrahydro-1-methyl-6,7-isoquinolinediol hydrobromide
- 1-Methyl-1,2,3,4-Tetrahydroisoquinoline-6,7-Diol Hydrobromide
- (1S)-6,7-dihydroxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium
- (1R)-6,7-dihydroxy-1-methyl-1,2,3,4-tetrahydroisoquinolinium
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Found 5 products.
1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrobromide
CAS:Formula:C10H14BrNO2Purity:95%Color and Shape:SolidMolecular weight:260.1277rac Salsolinol, Hydrobromide
CAS:rac Salsolinol, Hydrobromide is a useful organic compound for research related to life sciences. The catalog number is T124585 and the CAS number is 59709-57-8.Formula:C10H14BrNO2Color and Shape:SolidMolecular weight:260.128rac Salsolinol, Hydrobromide
CAS:Controlled Product<p>Stability Store in freezer at -20°C<br>Applications Salsolinol is derived from the neurotransmitter dopamine and acetaldehyde. Interest in this molecule comes from studies suggesting that it might be involved in alcohol addiction, as acetaldehyde is both a well recognized substrate for the Pictet-Spengler reaction and the primary metabolite of ethanol in the liver. It has further been suggested that acetaldehyde formed as a result of alcohol consumption might induce central changes in the metabolism of dopamine.<br>References J. Pharmacol. Exp. Ther., 174, 401 (1970); Science, 167, 1749 (1970); Science, 167, 1005 (1970); Aust. J. Chem., 41, 483 (1988)<br></p>Formula:C10H13NO2·BrHColor and Shape:NeatMolecular weight:260.13(+/-)-Salsolinol hydrobromide - Bio-X ™
CAS:<p>This product is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.</p>Formula:C10H14BrNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:260.13 g/mol(+/-)-Salsolinol hydrobromide
CAS:<p>(+/-)-Salsolinol hydrobromide is a chemical compound derived from the condensation of dopamine and acetaldehyde. This compound occurs naturally in the brain and certain fermented beverages, influencing neurological pathways. As a dopaminergic compound, it affects dopaminergic neurons by stimulating or inhibiting dopamine receptors, depending on the context of its application.The interest in (+/-)-Salsolinol hydrobromide centers around its potential involvement in neurodegenerative conditions such as Parkinson's disease. It is studied for its role in modulating dopamine metabolism and its impact on dopaminergic tone. The compound is also researched for its contribution to the addictive properties observed in alcohol consumption, given its formation during the metabolic processes initiated by alcohol intake.As a research tool, (+/-)-Salsolinol hydrobromide aids in understanding the interactions between neurotransmitter systems and their implications in neuropsychiatric disorders. Ongoing studies aim to elucidate its precise function, contributing to broader insights into the development of therapeutic targets for related pathological states.</p>Formula:C10H14BrNO2Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight:260.13 g/mol



