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1H-Indole-2-carboxylic acid, 3-(4-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141306-66-3

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141306-66-3 Usage

Molecular weight

284.28 g/mol

Structure

Indole-2-carboxylic acid derivative with a 4-fluorophenyl group

Type of compound

Heterocyclic organic compound

Usage

Synthesis of pharmaceuticals and agrochemicals

Potential applications

Medicine, agriculture, and material science

Importance

Valuable building block for drug and agrochemical development, versatile intermediate in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 141306-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141306-66:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*6)+(1*6)=93
93 % 10 = 3
So 141306-66-3 is a valid CAS Registry Number.

141306-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-fluorophenyl)-1H-indole-2-carboxylic acid

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:141306-66-3 SDS

141306-66-3Relevant academic research and scientific papers

BACTERIAL EFFLUX PUMP INHIBITORS

-

Page/Page column 75; 78, (2018/12/13)

Disclosed herein are compounds of formula I and salts thereof. Also disclosed are compositions comprising compounds of formula I and methods using compounds of formula I.

Fused lactones as a route to functionalized 1-substituted indoles

Schuster,Coppola

, p. 1381 - 1384 (2007/10/02)

Indole lactones 8 and 14 were synthesized as a means of functionalizing the 1-isopropyl substituent of the indole nucleus. Lactone 8, upon reduction with diisobutylaluminum hydride, produces lactol 9 which behaves like a masked hydroxy aldehyde and underg

Selective, Centrally Acting Serotonin 5-HT2 Antagonists. 2. Substituted 3-(4-Fluorophenyl)-1H-indoles

Andersen, Kim,Perregaard, Jens,Arnt, Joern,Nielsen, Joern Bay,Begtrup, Mikael

, p. 4823 - 4831 (2007/10/02)

A series of 3-(4-fluorophenyl)-1H-indoles substituted in the 1-position with 4-piperidinyl, 1,2,3,6-tetrahydro-4-pyridinyl, and 4-piperazinyl was synthesized. By variation of the substituents in the benzene part of the indole nucleus in 1-2-4-3-(4-fluo

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