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2-(5-nitro-1H-indol-3-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41339-64-4

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41339-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41339-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,3 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41339-64:
(7*4)+(6*1)+(5*3)+(4*3)+(3*9)+(2*6)+(1*4)=104
104 % 10 = 4
So 41339-64-4 is a valid CAS Registry Number.

41339-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-nitro-1H-indol-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names 5-Nitro-1H-indole-3-ethanol

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:41339-64-4 SDS

41339-64-4Relevant academic research and scientific papers

E-SELECTIN ANTAGONISTS

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Page/Page column 47, (2012/04/04)

Compounds, compositions and methods are provided for inhibiting in vitro and in vivo processes mediated by E-selectin binding. More specifically, particular glycomimetic compounds are described, wherein the compounds are E- selectin antagonists.

A fragment-based in situ combinatorial approach to identify high-affinity ligands for unknown binding sites

Shelke, Sachin V.,Cutting, Brian,Jiang, Xiaohua,Koliwer-Brandl, Hendrik,Strasser, Daniel S.,Schwardt, Oliver,Kelm, Soerge,Ernst, Beat

supporting information; experimental part, p. 5721 - 5725 (2010/11/02)

[Figure Presented] In the lead: The title method for the identification of ligands is particularly useful for binding sites where little or no structural information is available. In a fragment-based approach, a suitable pair of first- and second-site ligands is identiled by NMR experiments. By applying a receptor-mediated in situ combinatorial approach, the two ligands are then linked to generate a new high-affinity lead structure (see picture).

First heterogeneous ligand- and salt-free larock indole Synthesis

Batail, Nelly,Bendjeriou, Anissa,Lomberget, Thierry,Barrett, Roland,Dufaud, Veronique,Djakovitch, Laurent

supporting information; experimental part, p. 2055 - 2062 (2009/12/26)

A new ligand- and salt-free procedure using heterogeneous palladium catalysts for the Larock indole and benzofuran synthesis is reported. After optimisation of the reaction conditions, good to high isolated yields have been achieved for a variety of structures. Recycling studies have shown that the palladium catalysts can be readily recovered and reused. Reactions and recovery of the palladium catalysts can be carried out in the presence of air, without any particular precaution.

ANTIMIGRAINE CYCLOBUTENEDIONE DERIVATIVES OF TRYPTAMINES

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, (2008/06/13)

A series of serotonergic 5-cyclobutenedionylamino-substituted tryptamine derivatives of Formula I is disclosed for use in the alleviation of vascular headaches. STR1 The formula I substituents, as further defined in the specification, are: R 1 is hydrogen, halogen, and alkyl; R 2 and R 3 can be hydrogen or alkyl; R 4 is hydrogen, alkyl, acyl or alkylsulfonyl; m is 0 to 3 and n is 1 to 5; and X is amino, alkoxy, hydrogen, alkyl, aryl or alkylaryl.

Indolylalkylpiperidines

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, (2008/06/13)

1-(Indolyl-3-alkyl)-3 or 4-(ureido or guanidino)-piperidines, e.g. those of the formula STR1 R= H; alkyl; free, etherified or esterified OH or SH; CF3, NO2 or NH2 m= 1-4; n= 2 or 3; X= O, S or NH acyl derivatives and salts thereof are antihypertensive agents.

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