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1-(3,4-dimethoxyphenyl)-2-methylpropan-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75561-47-6

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75561-47-6 Usage

Type of drug

Synthetic psychoactive drug and substituted amphetamine

Derivative of

Amphetamine

Similar properties to

MDMA and mescaline

Effects on the body

Hallucinogenic and stimulant compound that affects the central nervous system

Leads to

Altered perceptions, mood changes, increased energy, and alertness

Primary use

Recreational purposes

Common forms

Tablet or powder

Legal status

Illegal in many countries due to potential for abuse and harmful side effects

Side effects

Anxiety, paranoia, and serotonin syndrome

Check Digit Verification of cas no

The CAS Registry Mumber 75561-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75561-47:
(7*7)+(6*5)+(5*5)+(4*6)+(3*1)+(2*4)+(1*7)=146
146 % 10 = 6
So 75561-47-6 is a valid CAS Registry Number.

75561-47-6Relevant academic research and scientific papers

Friedel-Crafts Acylation with N-(Trifluoroacetyl)-α-amino Acid Chlorides. Application to the Preparation of β-Arylalkylamines and 3-Substituted 1,2,3,4-Tetrahydroisoquinolines

Nordlander, Eric J.,Payne, Mark J.,Njoroge, George F.,Balk, Michael A.,Laikos George D.,Vishwanath, Vasanth M.

, p. 4107 - 4111 (2007/10/02)

Several N-(trifluoroacetyl)-α-amino acid chlorides have been reacted with benzene, anisole, and veratrole in the presence of AlCl3 or SnCl4 to produce the corresponding aromatic ketones in fair to high yields.The products are reductible under neutral or acidic conditions to the corresponding N-(trifluoroacetyl)-β-hydroxy-β-arylakylamines or N-(trifluoroacetyl)-β-arylalkylamines.The latter can be readily detrifluoroacetylated by mild basic hydrolysis and thence converted to the corresponding 3-substituted 1,2,3,4-tetrahydroisoquinolines by condensation with formaldehyde.

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