1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride

Product Name 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride
Alternate Names Phenylephrine Impurities, Impurities of Phenylephrine
CAT No. CS-O-11270
CAS No. 57196-61-9
Category Impurities
Stock IN-Stock
Mol. Wt. 215.68 g/mol
Mol. For. C₁₀H₁₄ClNO₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Phenylephrine
Purity 98.24
Smileys C[NH+]1CC(C2=C(C1)C=CC(=C2)O)O.[Cl-]
Canonical Smiles C[NH+]1CC(C2=C(C1)C=CC(=C2)O)O.[Cl-]
InchIKey NQWCCJZOYHZSNW-UHFFFAOYSA-N
Inchl InChI=1S/C10H13NO2.ClH/c1-11-5-7-2-3-8(12)4-9(7)10(13)6-11;/h2-4,10,12-13H,5-6H2,1H3;1H
IUPAC 2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium-4,6-diol;chloride
Controlled No
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1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride is a chemical compound that is commonly used in medical research. It is also referred to as THIQ or TIQ. This compound is a derivative of isoquinoline and has a molecular formula of C11H13NO3.HCl. It is a white crystalline powder that is soluble in water and ethanol. THIQ has been found to have a variety of potential medical applications due to its ability to act as an agonist at certain receptors in the brain. Specifically, it is a selective agonist for the dopamine D3 receptor, which is involved in regulating reward and addiction pathways in the brain. Research has shown that THIQ may have potential therapeutic benefits in the treatment of addiction and other psychiatric disorders. In addition to its potential medical applications, THIQ is also used in chemical and pharmaceutical research as a building block for the synthesis of other compounds. It can be synthesized from a number of different starting materials, and its chemical properties make it a versatile intermediate in the synthesis of other isoquinoline derivatives. Overall, 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride is a valuable compound with a wide range of potential applications in both medical and chemical research. Its unique chemical properties and selective receptor activity make it a valuable tool for understanding the complex workings of the brain and developing new treatments for a variety of disorders.

Related Compounds

Phenylephrine isoquinoline 4,6-diol analog | Phenylephrine EP Impurity C HCl | Phenylephrine EP Impurity E | Phenylephrine Impurity 4 | N-Nitroso Phenylephrine (Mixture of Isomers) | rac Benzyl Phenylephrine | Phenylephrine maleic acid adduct | Phenylephrine Impurity D | Phenylephrine Impurity 33 | Phenylephrine Impurity-37 | Phenylephrine Impurity C | D-Phenylephrine sulfonate | Phenylephrine Impurity 29 | L-Phenylephrine sulfonate | Phenylephrine EP Impurity A | Phenylephrine EP Impurity C TFA salt | Phenylephrine Impurity-41 | Phenylephrine D-(+)-glucose Adduct | Phenylephrine impurity 43 | Phenylephrine related compound F | Phenylephrine Citrate Adduct -2 | Phenylephrine Impurity 26 | Phenylephrine Impurity 38 | Phenylephrine Impurity 20 | rac 2-Bromo Phenylephrine Hydrochloride | Phenylephrine Impurity 12 | Phenylephrine Impurity-40 | N-acetylphenylephrine | Phenylephrine Impurity 5 | Phenylephrine isoquinolinone analog | Phenylephrine Impurity 9 | Phenylephrine Impurity-39 | O-Acetyl-(R)-phenylephrine Hydrochloride | N-(2-Succinyl) Phenylephrine |

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