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103205-15-8

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103205-15-8 Usage

Description

1-(1H-INDOL-3-YL)-ETHANOL, a derivative of the indole compound, is a heterocyclic aromatic chemical compound with the molecular formula C10H11NO. It presents as a pale yellow solid at room temperature and exhibits solubility in organic solvents. 1-(1H-INDOL-3-YL)-ETHANOL has garnered interest due to its potential pharmaceutical properties, particularly its interaction with serotonin receptors, positioning it as a candidate for the treatment of neurological disorders and psychiatric conditions. Furthermore, it is also considered for its utility as a chiral resolving agent and as a building block in the synthesis of other organic compounds. The exploration of its mechanism of action and applications is ongoing, revealing 1-(1H-INDOL-3-YL)-ETHANOL as a promising substance in the realms of medicine, chemistry, and pharmacology.

Uses

Used in Pharmaceutical Industry:
1-(1H-INDOL-3-YL)-ETHANOL is used as a potential therapeutic agent for neurological disorders and psychiatric conditions due to its effects on serotonin receptors, which are integral to mood regulation and various cognitive functions.
Used in Chemical Synthesis:
1-(1H-INDOL-3-YL)-ETHANOL is utilized as a chiral resolving agent, playing a crucial role in the separation of enantiomers, which is essential for the production of pure compounds with specific biological activities.
Used in Organic Chemistry:
1-(1H-INDOL-3-YL)-ETHANOL serves as a building block for the synthesis of other organic compounds, contributing to the development of new molecules with potential applications in various fields, including pharmaceuticals, materials science, and agrochemicals.

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.

103205-15-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-indol-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names Indole-3-methyl carbinol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:103205-15-8 SDS

103205-15-8Downstream Products

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.

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