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1-(5,6-dimethoxy-1H-indol-3-yl)-N,N-dimethylmethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5446-82-2

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5446-82-2 Usage

Chemical Class

Phenethylamine and substituted phenethylamine

Structural Relation

Related to psychedelic drugs like LSD and mescaline

Usage

Recreational use for hallucinogenic effects

Effects

Intense visual and auditory hallucinations, altered perceptions of time and space

Potential for Abuse

High

Adverse Effects

Cardiovascular complications, seizures, and other physical and psychological effects

Legal Status

Schedule I controlled substance in the United States

Legal Restrictions

Illegal to manufacture, distribute, or possess in the United States

Check Digit Verification of cas no

The CAS Registry Mumber 5446-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5446-82:
(6*5)+(5*4)+(4*4)+(3*6)+(2*8)+(1*2)=102
102 % 10 = 2
So 5446-82-2 is a valid CAS Registry Number.

5446-82-2Downstream Products

5446-82-2Relevant academic research and scientific papers

Studies on the Chemical Reactivity of the Quinone Methide Derived from the Oxidative Cyclization of α-Methyl-3,4-dihydroxyphenylalanine Ethyl Ester

Cheng, Alice C.,Shulgin, Alexander T.,Castagnoli, Neal

, p. 5258 - 5262 (1982)

Air oxidation of the ethyl ester of (S)-α-methyl-3,4-dihydroxyphenylalanine generates the corresponding cyclic quinone methide which proved to be unreactive toward nucleophiles.Under a variety of reaction conditions the quinone methide rearranged to an indole, the structure of which was established by an independent synthesis to be ethyl 5,6-dihydroxy-2-methylindole-3-carboxylate.

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