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1H-Indole-4-carboxylic acid, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84401-11-6

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84401-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84401-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,0 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84401-11:
(7*8)+(6*4)+(5*4)+(4*0)+(3*1)+(2*1)+(1*1)=106
106 % 10 = 6
So 84401-11-6 is a valid CAS Registry Number.

84401-11-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 1H-indole-4-carboxylate

1.2 Other means of identification

Product number -
Other names benzyl indole-4-carboxylate

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:84401-11-6 SDS

84401-11-6Relevant academic research and scientific papers

Preparation method 3 - (trifluoromethyl) -4 -indolinic acid

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Paragraph 0059-0061; 0072-0073, (2021/09/15)

The invention discloses a preparation method of 3 - (trifluoromethyl) -4 -indolinic acid. The method comprises the following steps: (1) protecting the indole 4 - formic acid through a benzyl protecting carboxylic acid to obtain the compound shown in the formula 1. (2): The compound represented by Formula 1 is protected by an amino group to obtain a compound represented by Formula 2. (3): The compound represented by Formula 2 is substituted with iodine to obtain a compound represented by Formula 3. (4): A compound represented by Formula 3 is mixed with a trifluoromethylation reagent to react to obtain a compound having the structure shown in Formula 4. (5) The compound of formula 4 was subjected to deamination protection and benzyl to give 3 - (trifluoromethyl) -4 -indolinic acid.

Discovery and evaluation of a series of 3-acylindole imidazopyridine platelet-activating factor antagonists

Curtin, Michael L.,Davidsen, Steven K.,Heyman, H. Robin,Garland, Robert B.,Sheppard, George S.,Florjancic, Alan S.,Xu, Lianhong,Carrera Jr., George M.,Steinman, Douglas H.,Trautmann, Jeff A.,Albert, Daniel H.,Magoc, Terrance J.,Tapang, Paul,Rhein, David A.,Conway, Richard G.,Luo, Gongjin,Denissen, Jon F.,Marsh, Kennan C.,Morgan, Douglas W.,Summers, James B.

, p. 74 - 95 (2007/10/03)

Studies conducted with the goal of discovering a second-generation platelet-activating factor (PAF) antagonist have identified a novel class of potent and orally active antagonists which have high aqueous solubility and long duration of action in animal m

Synthesis of N-Alkyl Derivatives of 4-(2'-Aminoethyl)indole

Cannon, Joseph G.,Demopoulos, Basil J.

, p. 1195 - 1199 (2007/10/02)

N-Substituted 4-(2'-aminoethyl)indoles are attainable in good yields from indole-4-acetic acid (2).Several methods of preparation for 2 were tried or considered.A new sequence involving Arndt-Eistert homologation of indole-4-carboxylic acid has been devis

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