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1-Propanone, 3-(dimethylamino)-1-(2-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

46394-28-9

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46394-28-9 Usage

Type

Synthetic cathinone

Classification

Stimulant, entactogen

Chemical relation

Related to cathinone, a stimulant found in the khat plant

Legal status

Controlled substance in many countries

Effects

Euphoria, increased heart rate, elevated blood pressure, changes in perception and mood, feelings of empathy and emotional openness, increased energy

Long-term use risks

Adverse effects on mental and physical health, potential for abuse and addiction.

Check Digit Verification of cas no

The CAS Registry Mumber 46394-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,3,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 46394-28:
(7*4)+(6*6)+(5*3)+(4*9)+(3*4)+(2*2)+(1*8)=139
139 % 10 = 9
So 46394-28-9 is a valid CAS Registry Number.

46394-28-9Relevant academic research and scientific papers

Metal-free synthesis of β-aminoketones by the reductive hydroamination of ynones

Fu, Rui,Liu, Yu,Wu, Tao,Zhang, Xinyu,Zhu, Yang,Luo, Jiangbin,Zhang, Zhengyu,Jiang, Yaojia

, p. 3525 - 3528 (2022/03/31)

This study describes a cascade method for the synthesis of β-aminoketones through the reductive hydroamination of alkynes under very mild metal-free conditions. It allows for the rapid conversion of ynones and amines into corresponding β-aminoketones with a broad substrate scope and diverse functionalities. This straightforward and easy-to-handle reaction process can be successfully applied for the synthesis of Proroxan and Propipocaine, offering a potential option for the synthesis of drug molecules with the β-aminoketone skeleton.

SMALL MOLECULE CMKLR1 ANTAGONISTS IN INFLAMMATORY DISEASE

-

Paragraph 0199; 0230; 0232; 0245, (2020/12/01)

α-NETA analogs are provided for the treatment of inflammatory disease.

NOVEL 5-HT2 ANTAGONISTS

-

Paragraph 0071, (2017/01/05)

The present invention relates to 1-amidino-3-aryl-2-pyrazoline derivatives of the general formula I The invention specifically relates to such derivatives which exhibit antagonizing activity towards serotonin 5-HT2B receptors. The present invention also relates to use of said compounds as a medicament and for the treatment of fibrosis, cardiovascular diseases, pain, IBD, and other inflammatory diseases, as well as pharmaceutical compositions comprising one or more of said compounds and methods of treatment.

GAMMA-DIKETONES AS WNT/BETA -CATENIN SIGNALING PATHWAY ACTIVATORS

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Paragraph 1714; 1715; 1716; 1727, (2014/09/03)

The present disclosure provides γ-diketones or analogs thereof, that activate Wnt/β-catenin signaling and thus treat or prevent diseases related to signal transduction, such as osteoporosis and osteoarthropathy; osteogenesis imperfecta, bone defects, bone fractures, periodontal disease, otosclerosis, wound healing, craniofacial defects, oncolytic bone disease, traumatic brain injuries or spine injuries, brain atrophy/neurological disorders related to the differentiation and development of the central nervous system, including Parkinson's disease, strokes, ischemic cerebral disease, epilepsy, Alzheimer's disease, depression, bipolar disorder, schizophrenia; otic disorders like cochlear hair cell loss; eye diseases such as age related macular degeneration, diabetic macular edema or retinitis pigmentosa and diseases related to differentiation and growth of stem cell, such as hair loss, hematopoiesis related diseases and tissue regeneration related diseases.

UROTENSIN II RECEPTOR MODULATORS

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Page 33-35, (2010/02/04)

Disclosed are compounds of Formula I, or salts or prodrugs thereof, complexed with a human urotensin II receptor as defined herein. Also disclosed are compounds of Formula II, or salts or prodrugs thereof, as defined herein. Also disclosed are methods of modulating the activity of a urotensin II receptor using a compound of Formula I, or a compound of Formula II, or salts or prodrugs thereof. In addition, methods of treating diseases related to the activity of urotensin II receptors are disclosed.

The Synthesis of Indan-1-ones and Isocoumarins

Carter, Rachel H.,Garson, Mary J.,Hill, Robert A.,Staunton, James,Sunter, David C.

, p. 471 - 479 (2007/10/02)

A flexible synthetic route leading via indan-1-ones to variously methylated and oxygenated isocoumarins is described.The indanones are prepared by alternative routes involving intramolecular Friedel-Crafts cyclisation of arylpropionic acids or pericyclic ring closure of acrylophenones.The influence of substitution on the rate of the pericyclic reaction is assessed.

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