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19499-82-2

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19499-82-2 Usage

Structure

A derivative of indole with a hydroxyl group attached to the 4th carbon and a dimethylaminoethyl group attached to the 5th carbon.

Functional groups

Hydroxyl (-OH) and dimethylaminoethyl (-N(CH3)2-CH2-).

Applications

Often used in organic synthesis and pharmaceutical research.

Potential applications

Neuroscience and psychiatry drug development.

Chemical and pharmacological properties

The attachment of the dimethylaminoethyl group to the indole ring can modify the compound's properties.

Check Digit Verification of cas no

The CAS Registry Mumber 19499-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19499-82:
(7*1)+(6*9)+(5*4)+(4*9)+(3*9)+(2*8)+(1*2)=162
162 % 10 = 2
So 19499-82-2 is a valid CAS Registry Number.

19499-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(dimethylamino)methyl]-1H-indol-4-ol

1.2 Other means of identification

Product number -
Other names 5-(N,N-dimethylaminomethyl)indol-4-ol

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:19499-82-2 SDS

19499-82-2Relevant articles and documents

Optimised synthesis and photochemistry of antenna-sensitised 1-acyl-7-nitroindolines

Papageorgiou, George,Corrie, John E.T.

, p. 609 - 616 (2007/10/03)

Benzophenone antenna-sensitised 1-acyl-7-nitroindolines show a significantly enhanced extent of photochemical cleavage in aqueous solution over their non-sensitised analogues and release the carboxylate derived from their 1-acyl group. The present work in

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