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1H-Indole-1-carboxamide, N,N-diethyl-3-(hydroxyphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105949-33-5

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105949-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105949-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,4 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105949-33:
(8*1)+(7*0)+(6*5)+(5*9)+(4*4)+(3*9)+(2*3)+(1*3)=135
135 % 10 = 5
So 105949-33-5 is a valid CAS Registry Number.

105949-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxyphenylmethyl)indole-1-carboxylic acid diethylamide

1.2 Other means of identification

Product number -
Other names -

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:105949-33-5 SDS

105949-33-5Relevant academic research and scientific papers

Automated generation and reactions of 3-hydroxymethylindoles in continuous-flow microreactors

Tricotet, Thomas,O'Shea, Donal F.

experimental part, p. 6678 - 6686 (2010/08/20)

An automated sequential approach for the generation and reactions of 3-hydroxymethylindoles in continuous-flow microreactors is described. Consecutive halogen-magnesium exchanges of four 3-iodoindoles followed by addition to three aldehydes provided twelv

SYNTHESIS OF 3-SUBSTITUTED INDOLES VIA N-ACYLINDOLIUM IONS

Comins, Daniel L.,Stroud, Eric D.

, p. 1869 - 1872 (2007/10/02)

3-Substituted N-(N'N'-diethylcarbamyl)indoles are prepared from indole-3-carboxaldehyde in good overall yield via N-acylindolium ion intermediates.

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