104599-04-4 Usage
1H-Indol-5-ol, 3-methyl-2-phenyl-1-(phenylmethyl)-
the chemical name of the compound
Tryptamine
common name for the compound
Psychoactive compound
a substance that affects the mind or emotions
Derivative of serotonin
a chemical compound that is structurally related to the neurotransmitter serotonin
Serotonergic psychedelic
a type of psychedelic drug that primarily affects the serotonin system in the brain
Schedule I controlled substance
a substance that is illegal to manufacture, distribute, or possess in the United States due to its high potential for abuse and lack of accepted medical use
Found in plants, fungi, and animals
the compound is naturally occurring in various organisms
Structural analogue of serotonin
the compound has a similar chemical structure to the neurotransmitter serotonin
Precursor in the synthesis of other psychoactive substances
the compound is used as a starting material in the production of other psychoactive substances, such as DMT and psychedelic phenethylamines
Hallucinogenic effects
the compound can cause changes in perception, mood, and thought
Used in spiritual practices and recreational drug use
the compound has been used for spiritual and recreational purposes due to its psychoactive effects.
Check Digit Verification of cas no
The CAS Registry Mumber 104599-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,9 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104599-04:
(8*1)+(7*0)+(6*4)+(5*5)+(4*9)+(3*9)+(2*0)+(1*4)=124
124 % 10 = 4
So 104599-04-4 is a valid CAS Registry Number.
104599-04-4Relevant academic research and scientific papers
2-Phenylindoles. Effect of N-Benzylation on Estrogen Receptor Affinity, Estrogenic Properties, and Mammary Tumor Inhibiting Activity
Angerer, Erwin von,Strohmeier, Josef
, p. 131 - 136 (2007/10/02)
Hydroxy-2-phenylindoles carrying substituted benzyl groups and similar substituents at the nitrogen were synthesized and tested for their ability to displace estradiol from its receptor. All of the derivatives tested exhibited high binding affinities for
