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N,N'-(1,4-phenylenebis(methan-1-yl-1-ylidene))dicyclohexanamine, also known as 4,4'-Methylenebis(N,N-dicyclohexylbenzenamine) or MDA, is an organic compound with the chemical formula C25H41N. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 65-67°C. MDA is a synthetic psychoactive drug that belongs to the phenethylamine class and is structurally similar to amphetamines. It acts as a central nervous system stimulant and has been used recreationally for its euphoric and hallucinogenic effects. However, it is also known for its potential neurotoxicity and has been classified as a Schedule I controlled substance in many countries due to its high potential for abuse and lack of accepted medical use.

3525-62-0

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3525-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3525-62-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3525-62:
(6*3)+(5*5)+(4*2)+(3*5)+(2*6)+(1*2)=80
80 % 10 = 0
So 3525-62-0 is a valid CAS Registry Number.

3525-62-0Upstream product

3525-62-0Relevant academic research and scientific papers

Novel Reaction between 3,4,5,6-Tetrachloro-1,2-benzoquinone and Bis-azomethines

Aly, Ashraf A.,Mohamed, Nasr K.,Hassan, Alaa A.,Mourad, Aboul-Fetouh E.

, p. 2249 - 2252 (1996)

3,4,5,6-Tetrachloro-1,2-benzoquinone (o-CHL) reacted with N,N1-dicyclohexyl-1,2-ethanediimine 1a to give a transient condensation product, which underwent [4 + 2]cycloaddition reaction with another molecule of 1a. In a different manner, utilizi

Exploration of imidazole and imidazopyridine dimers as anticancer agents: Design, synthesis, and structure–activity relationship study

Meenakshisundaram, Sangeetha,Manickam, Manoj,Pillaiyar, Thanigaimalai

, (2019/11/03)

Dimerization of proteins/receptors plays a critical role in various cellular processes, including cell proliferation and differentiation. Therefore, targeting such dimeric proteins/receptors by dimeric small molecules could be a potential therapeutic appr

The stereochemical behavior of terephthalic schiff bases in addition of dialkyl or diaryl phosphites

Lewkowski, Jaroslaw

, p. 179 - 195 (2007/10/03)

Addition of dialkyl (or diaryl) phosphites to N-alkyl terephthalic Schiff bases led exclusively to a meso-form but addition to N-aryl terephthalic Schiff bases depended on the substituent of the aryl group. Semi-empirical calculations were involved to fin

SYNTHESIS, NMR INVESTIGATION AND FAB-MS CHARACTERIZATION OF 1-AMINO-2-ARYLMETHYL-DIPHOSPHONATE ESTERS

Failla, Salvatore,Finocchiaro, Paolo,Hagele, Gerhard,Rapisardi, Roberto

, p. 79 - 90 (2007/10/02)

Variously substituted amino aryl-methyl-diphosphonate ethyl esters have been prepared in good yields by adding diethyl phosphonate to the corresponding Schiff bases.All compounds were characterized by NMR and MS-FAB techniques, which reveal the presence o

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