CAS 51-02-5

2-Naphthalenemethanol, α-[[(1-methylethyl)amino]methyl]-, hydrochloride (1:1)

Description:

2-Naphthalenemethanol, α-[[(1-methylethyl)amino]methyl]-, hydrochloride (1:1), commonly known as a derivative of naphthalene, is a chemical compound characterized by its naphthalene backbone with a hydroxymethyl group and an isopropylamino substituent. This compound typically appears as a white to off-white crystalline solid and is soluble in water due to the presence of the hydrochloride salt form, which enhances its solubility compared to its free base. It exhibits properties typical of both aromatic compounds and alcohols, including potential biological activity. The presence of the amino group suggests that it may engage in hydrogen bonding, influencing its reactivity and interactions with biological systems. This compound is often studied for its pharmacological properties, particularly in relation to its potential use in medicinal chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper laboratory practices should be followed when working with this substance.

Formula: C₁₅H₂₀ClNO

InChI: InChI=1/C15H19NO.ClH/c1-11(2)16-10-15(17)14-8-7-12-5-3-4-6-13(12)9-14;/h3-9,11,15-17H,10H2,1-2H3;1H

InChI key: InChIKey=QONLGXRPRAIDGI-UHFFFAOYSA-N

SMILES: C(CNC(C)C)(O)C1=CC2=C(C=C1)C=CC=C2.Cl

Synonyms:

• 1-(Naphthalen-2-Yl)-2-(Propan-2-Ylamino)Ethanol
• 1-(Naphthalen-2-Yl)-2-(Propan-2-Ylamino)Ethanol Hydrochloride (1:1)
• 2-Isopropylamino-1-(2-naphthyl)ethanol hydrochloride
• 2-Naphthalenemethanol, alpha-(((1-methylethyl)amino)methyl)-, hydrochloride
• 2-Naphthalenemethanol, α-[(isopropylamino)methyl]-, hydrochloride
• 2-Naphthalenemethanol, α-[[(1-methylethyl)amino]methyl]-, hydrochloride
• 2-Naphthalenemethanol, α-[[(1-methylethyl)amino]methyl]-, hydrochloride (1:1)
• <span class="text-smallcaps">DL</span>-Pronethalol hydrochloride
• Alderlin hydrochloride
• Ay 6204
• Ccris 534
• DL-Pronethalol hydrochloride
• Ici 38174
• Naphthalenemethanol, alpha-((isopropylamino)methyl)-, hydrochloride
• Naphthylisoproterenol hydrochloride
• Nethalide hydrochloride
• Pronetalol
• Pronetalol HCl
• Pronetalol hydrochloride
• Unii-Xbp4Rt1Imq
• alpha-(((1-Methylethyl)amino)methyl)-2-naphthalenemethanol, hydrochloride
• alpha-((Isopropylamino)methyl)-2-naphthalenemethanol hydrochloride
• Pronethalol hydrochloride
• alpha-((isopropylamino)methyl)-naphthalenemethanohydrochloride
• alpha-((isopropylamino)methyl)-2-naphthalenemethanolhydrochloride
• ici38174
• PronethalolHCl
• 1-naphthalen-2-yl-2-(propan-2-ylamino)ethanol hydrochloride
• alderlinhydrochloride
• naphthylisoproterenolhydrochloride

2-Isopropylamino-1-(2-naphthyl)ethanol hydrochloride

CAS: 51-02-5

Formula: C₁₅H₂₀ClNO

Purity: 98%

Color and Shape: Solid

Molecular weight: 265.7784

Ref: IN-DA00DGSC

(+/-)-Pronethalol HCl

CAS: 51-02-5

Pronethalol is a dpp-iv inhibitor that binds to the enzyme as a competitive antagonist. It has been shown to reduce blood pressure in rats with chronic pulmonary hypertension. Pronethalol also has biphasic effects on heart rate, increasing it at low doses and decreasing it at high doses. This effect may be due to its ability to block alpha-adrenergic receptors, which are responsible for vasoconstriction and increased heart rate. Pronethalol has also been shown to significantly inhibit aminotransferase activity in mice, which may be due to its inhibition of pyridoxine 4'-phosphate (PNP) reductase and pyridoxine 5'-phosphate (PNP) oxidase. The test compound is a white crystalline solid that can be detected by fluorescence detector or chromatographic methods.

Formula: C₁₅H₁₉NO·HCl

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 265.78 g/mol

Ref: 3D-FP27185

Pronethalol hydrochloride

CAS: 51-02-5

β-adrenergic antagonist

Formula: C₁₅H₂₀ClNO

Purity: 98%

Color and Shape: Solid

Molecular weight: 265.78

Ref: TM-T23187

Pronethalol Hydrochloride

CAS: 51-02-5

Color and Shape: Neat

Ref: 61-FOR0719.00