103205-15-8 Usage
General Description
1-(1H-Indol-3-yl)-ethanol is a chemical compound with a molecular formula C10H11NO. It is a derivative of the indole compound, which is a heterocyclic aromatic ring structure. 1-(1H-INDOL-3-YL)-ETHANOL appears as a pale yellow solid at room temperature and is soluble in organic solvents. It has been studied for its potential pharmaceutical properties, including its effects on serotonin receptors and its potential as a therapeutic agent for neurological disorders and psychiatric conditions. Additionally, it has also been investigated for its potential as a chiral resolving agent and as a building block for the synthesis of other organic compounds. While its precise mechanism of action and full range of potential applications are still being explored, 1-(1H-indol-3-yl)-ethanol shows promise in a variety of fields, including medicine, chemistry, and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 103205-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103205-15:
(8*1)+(7*0)+(6*3)+(5*2)+(4*0)+(3*5)+(2*1)+(1*5)=58
58 % 10 = 8
So 103205-15-8 is a valid CAS Registry Number.
103205-15-8Relevant articles and documents
Iron(II) chloride-1,1′-binaphthyl-2,2′-diamine (FeCl 2-BINAM) complex catalyzed domino synthesis of bisindolylmethanes from indoles and primary alcohols
Badigenchala, Sindhura,Ganapathy, Dhandapani,Das, Ankita,Singh, Rahul,Sekar, Govindasamy
, p. 101 - 109 (2014)
Biologically important bisindolylmethanes are synthesized in a domino fashion by using an iron(II) chloride-(±)-1,1′-binaphthyl-2, 2′-diamine [FeCl2-(±)-BINAM] complex as the catalyst. This method proceeds via oxidation of a primary alcohol into the corresponding aldehyde followed by nucleophilic addition of an indole in the presence of the catalyst. A reaction intermediate is synthesized separately and converted into the bisindolylmethane product under the same reaction conditions as support for the proposed mechanism. Georg Thieme Verlag Stuttgart · New York.
