Welcome to LookChem.com Sign In|Join Free
  • or
1-(1-methyl-2-phenylethyl)-4-piperidone, also known as MDPK, is a chemical compound belonging to the piperidones class. With the molecular formula C16H21NO, MDPK is a psychoactive synthetic stimulant structurally related to the cathinone class of compounds. It functions as a norepinephrine-dopamine reuptake inhibitor, increasing the levels of dopamine and norepinephrine in the brain, which leads to its stimulating and euphoric effects.

16771-90-7

Post Buying Request

16771-90-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

16771-90-7 Usage

Uses

Used in Recreational Drug Industry:
1-(1-methyl-2-phenylethyl)-4-piperidone is used as a recreational drug for its stimulating and euphoric effects. As a norepinephrine-dopamine reuptake inhibitor, it increases the levels of these neurotransmitters in the brain, leading to the desired psychological outcomes. However, it is important to note that the use of MDPK as a recreational drug can have potential health risks and legal implications.

Check Digit Verification of cas no

The CAS Registry Mumber 16771-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,7 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16771-90:
(7*1)+(6*6)+(5*7)+(4*7)+(3*1)+(2*9)+(1*0)=127
127 % 10 = 7
So 16771-90-7 is a valid CAS Registry Number.

16771-90-7Downstream Products

16771-90-7Relevant academic research and scientific papers

PESTICIDAL SUBSTITUTED PIPERIDINES

-

Page/Page column 51; 62, (2008/06/13)

The invention relates to the use of piperidine derivatives encompassed from the general formula (I) for the control of pests, including arthropods and helminths, and a method for the control of pests.

STERIC CONTROL OF THE ASYMMETRIC SYNTHESIS OF N-SUBSTITUTED 2-METHYL-4-PIPERIDONES

Grishina, G. V.,Potapov, V. M.,Abdulganeeva, S. A.,Korchagina, E. Yu.

, p. 1355 - 1362 (2007/10/02)

Transmission of the iodomethylate of 1,2-dimethyl-4-piperidone by (S)-sec-butylamine gives 1-(S-sec-butyl)-2S-methyl-4-piperidone in 33percent optical yield while transamination by (S)-1-methyl-2-phenylethylamine gives a 1:1 diastereomeric mixture of 1-(1-methyl-2-phenylethyl)-2-methyl-4-piperidone.The decrease in the optical yield is related to the facile opening of the piperidone ring at the C-N bond with subsequent recyclization.The 13C NMR data indicate that all the diastereomers of the 4-piperidones obtained are in the chair conformation with predominantly equatorial orientation of the methyl group at C(2).The chi ral optical properties were studied and the absolution configurations of the 4-piperidones were established.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 16771-90-7