111098-37-4

Basic information

• Product Name: N-(1,2-Dimethylpropyl)-2-pyridinamine
• Synonyms: N-(1,2-Dimethylpropyl)-2-pyridinamine
• CAS NO: 111098-37-4
• Molecular Formula: C10H16N2
• Molecular Weight: 164.25
• Mol File: 111098-37-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 257 ºC
• Flash Point: 109 ºC
• Appearance: /
• Density: 0.972
• Vapor Pressure: 0.0145mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-(1,2-Dimethylpropyl)-2-pyridinamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1,2-Dimethylpropyl)-2-pyridinamine(111098-37-4)
• EPA Substance Registry System: N-(1,2-Dimethylpropyl)-2-pyridinamine(111098-37-4)

Safety Data

• Hazardous Substances Data: 111098-37-4(Hazardous Substances Data)

Usage

General Description

N-(1,2-Dimethylpropyl)-2-pyridinamine, also known as lorpiprazole, is a chemical compound used as an antipsychotic medication. It acts as a dopamine D2 receptor antagonist and serotonin 5-HT2A receptor antagonist, and is believed to help regulate mood and behavior by altering the balance of neurotransmitters in the brain. Lorpiprazole is used to treat conditions such as schizophrenia and bipolar disorder. It is typically administered orally in the form of tablets or capsules, and its dosage must be carefully monitored to avoid potential side effects such as drowsiness, dizziness, and weight gain.

InChI:InChI=1/C10H16N2/c1-8(2)9(3)12-10-6-4-5-7-11-10/h4-9H,1-3H3,(H,11,12)

Upstream product

• 504-29-0 2-aminopyridine 
• 563-80-4 3-methyl-butan-2-one 
• 917-64-6 methyl magnesium iodide 
• 111098-27-2 2-<1-(benzotriazol-1-yl)-2-methylpropylamino>pyridine 

Relevant articles and documents

AROMATIC COMPOUND

Provided is a novel aromatic ring compound having a GPR40 agonist activity and a GLP-1 secretagogue action. A compound represented by the formula: wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity and a GLP-1 secretagogue action, is useful for the prophylaxis or treatment of cancer, obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia and the like, and affords superior efficacy.

The Chemistry of N-Substituted Benzotriazoles. Part 4. A Novel and Versatile Method for the Mono-N-alkylation of Aromatic and Heteroaromatic Amines

Mono-N-alkylation of aromatic and heteroaromatic amines is achieved in high yield by NaBH4 reduction of the adducts formed from benzotriazole, aliphatic aldehydes and the amines.Reaction of the same adducts with Grignard reagents gives N-(secondary alkyl)arylamines.Carboxy groups need no protection and nitro groups are unaffected.Adenine is mono-N-alkylated in high yield.