179899-22-0

Basic information

• Product Name: 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine
• Synonyms: 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine;7-aMino-1,2,3,4-tetrahydro-2,2-diMethylquinoline;2,2-diMethyl-1,2,3,4-tetrahydro-quinolin-7-ylaMine
• CAS NO: 179899-22-0
• Molecular Formula: C11H16N2
• Molecular Weight: 176.25814
• Mol File: 179899-22-0.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine(179899-22-0)
• EPA Substance Registry System: 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine(179899-22-0)

Safety Data

• Hazardous Substances Data: 179899-22-0(Hazardous Substances Data)

Usage

General Description

2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine, also known as 2,2-Dimethyl-7-methyl-1,2,3,4-tetrahydroquinoline-1-amine, is an organic compound with the molecular formula C14H21N. It is a derivative of quinoline and is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. This chemical is also used as an intermediate for organic synthesis and can be found in some research and development applications. Additionally, 2,2-DiMethyl-1,2,3,4-tetrahydroquinolin-7-aMine has potential biological activities and is a promising substance for further investigation in the field of medicinal chemistry.

Upstream product

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Relevant articles and documents

1,2,3,4-tetrahydroquinoline compound and synthetic method and application thereof

The invention relates to 1,2,3,4-tetrahydroquinoline compound and a synthetic method and application thereof. In a structure formula of the compound, the R1 is nitro or trifluoromethyl or 3-nitrophenylnitrobenzene sulfonyl or cyano, the R2 is hydrogen or methyl, the R3 is methyl formate or butyl formate, and the R4 is methyl. An aromatic ring of the 1,2,3,4-tetrahydroquinoline compound contains a series of electron withdrawing groups. The synthetic method is simple, economical, environment-friendly, easy to operate, easy to control, higher in product purity and yield and good in development prospect in industrial production; in addition, the synthetic method is also a novel synthetic method in atom economy; furthermore, the 1,2,3,4-tetrahydroquinoline compound can serve as intermediate to be used for preparing antagonist medicine.

Switching Androgen Receptor Antagonists to Agonists by Modifying C-Ring Substituents on Piperidinoquinolinone

New nonsteroidal human androgen receptor (hAR) agonists were developed from an hAR antagonist pharmacophore, 2(1H-piperidinoquinolinone. (+/-)-trans-7,8-diethyl-4-trifluoromethyl-2(1H)-piperidinoquinolinone was synthesized and demonstrated p

Tricyclic steroid receptor modulator compounds and methods

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.