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125453-50-1

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125453-50-1 Usage

Description

(2-phenylpropyl)(propan-2-yl)amine, commonly known as methamphetamine, is a potent central nervous system stimulant with strong addictive properties. It is a white, odorless crystalline powder that belongs to the amphetamine class of drugs and is illicitly produced and used for its euphoric effects.

Uses

Used in Pharmaceutical Industry:
Methamphetamine is used as a stimulant medication for the treatment of attention deficit hyperactivity disorder (ADHD) and obesity, due to its ability to increase alertness, focus, and energy levels.
Used in Recreational Drug Use:
Methamphetamine is used as a recreational substance for its euphoric effects, leading to feelings of increased energy, alertness, and pleasure. However, its use is associated with severe physical and psychological dependence, as well as a range of adverse health effects, including cardiovascular issues, neurological damage, and mental health disorders.
Used in Criminal Activities:
The illicit production and use of methamphetamine have led to widespread social and health concerns, as well as an increased risk of engaging in risky behaviors and criminal activities. Methamphetamine is classified as a controlled substance in many countries and is illegal to possess, manufacture, or distribute without proper authorization.

Check Digit Verification of cas no

The CAS Registry Mumber 125453-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,5 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125453-50:
(8*1)+(7*2)+(6*5)+(5*4)+(4*5)+(3*3)+(2*5)+(1*0)=111
111 % 10 = 1
So 125453-50-1 is a valid CAS Registry Number.

125453-50-1Downstream Products

125453-50-1Relevant articles and documents

Selective one-pot synthesis of symmetrically and unsymmetrically substituted amines via rhodium catalysed multiple alkylations of ammonia or primary amines under hydroformylation conditions

Rische, Thorsten,Kitsos-Rzychon, Beate,Eilbracht, Peter

, p. 2723 - 2742 (1998)

Symmetrically and unsymmetrically substituted secondary and tertiary amines are selectively prepared in high yields by a one-pot multiple alkylation procedure from ammonia or primary amines with styrenes and/or cyclic olefins, carbon monoxide and hydrogen

Synthesis of amines from alcohols in a nonepimerizing one-pot sequence - Synthesis of bioactive compounds: Cinacalcet and dexoxadrol

Guerin, Claire,Bellosta, Veronique,Guillamot, Gerard,Cossy, Janine

experimental part, p. 2990 - 3000 (2012/07/13)

A general, mild, and chemoselective one-pot oxidation/imine-iminium formation/nucleophilic addition sequence allowing the N-alkylation of amines by alcohols is described. This metal-free, one-pot sequence produced a wide variety of amines in good yields and diastereoselectivities, without the epimerization of the enantioenriched amines or alcohols involved in the process. This method was applied to the syntheses of the biologically active compounds cinacalcet and dexoxadrol. Copyright

Zwitterionic rhodium complex catalyzed hydroaminomethylation of arylethylenes

Lin, Yong-Shou,El Ali, Bassam,Alper, Howard

, p. 2423 - 2425 (2007/10/03)

The hydroaminomethylation of arylethylenes can be achieved in high regioselectivity using the zwitterionic rhodium complex [Rh+(cod)(η6-PhBPh3)-] (1) as the catalyst under relatively mild conditions.

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