15700-23-9 Usage
Uses
Used in Pharmaceutical Research:
1H-Indol-7-ol,3-(2-aminoethyl)-(9CI) is used as a key intermediate in the development of drugs targeting serotonin receptors and other neurological pathways. Its unique structure allows for the modulation of these pathways, which can lead to the creation of new treatments for neurological disorders.
Used in Organic Synthesis:
In the field of organic synthesis, 1H-Indol-7-ol,3-(2-aminoethyl)-(9CI) serves as a valuable building block for the creation of more complex organic molecules. Its reactivity and functional groups make it a useful component in the synthesis of various organic compounds.
Used in Dyes and Pigments Production:
Due to its aromatic structure, 1H-Indol-7-ol,3-(2-aminoethyl)-(9CI) may also have uses in the production of dyes and pigments. Its ability to impart color and its chemical properties make it a candidate for use in the development of new dyes and pigments for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 15700-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,0 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15700-23:
(7*1)+(6*5)+(5*7)+(4*0)+(3*0)+(2*2)+(1*3)=79
79 % 10 = 9
So 15700-23-9 is a valid CAS Registry Number.
15700-23-9Relevant academic research and scientific papers
Biocatalytic Production of Psilocybin and Derivatives in Tryptophan Synthase-Enhanced Reactions
Blei, Felix,Baldeweg, Florian,Fricke, Janis,Hoffmeister, Dirk
, p. 10028 - 10031 (2018/07/29)
Psilocybin (4-phosphoryloxy-N,N-dimethyltryptamine) is the main alkaloid of the fungal genus Psilocybe, the so-called “magic mushrooms.” The pharmaceutical interest in this psychotropic natural product as a future medication to treat depression and anxiety is strongly re-emerging. Here, we present an enhanced enzymatic route of psilocybin production by adding TrpB, the tryptophan synthase of the mushroom Psilocybe cubensis, to the reaction. We capitalized on its substrate flexibility and show psilocybin formation from 4-hydroxyindole and l-serine, which are less cost-intensive substrates, compared to the previous method. Furthermore, we show enzymatic production of 7-phosphoryloxytryptamine (isonorbaeocystin), a non-natural congener of the Psilocybe alkaloid norbaeocystin (4-phosphoryloxytryptamine), and of serotonin (5-hydroxytryptamine) by means of the same in vitro approach.
