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ethyl 1-indolinecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61589-17-1

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61589-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61589-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61589-17:
(7*6)+(6*1)+(5*5)+(4*8)+(3*9)+(2*1)+(1*7)=141
141 % 10 = 1
So 61589-17-1 is a valid CAS Registry Number.

61589-17-1SDS

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 ethyl 2,3-dihydroindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl-indolin-1-carboxylat

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:61589-17-1 SDS

61589-17-1Relevant academic research and scientific papers

Cp*CoIII-Catalyzed C(7)–H Bond Annulation of Indolines with Alkynes

Garai, Bholanath,Mandal, Rajib,Sundararaju, Basker

, p. 9407 - 9417 (2021)

An efficient protocol for the synthesis of biologically essential pyrroloquinolinones has been developed under Cp*CoIII catalysis, which involves a cascade reaction of C(7)-H alkenylation with alkynes followed by nucleophilic addition. A wide variety of internal alkynes including enyne, diyne, and ynamide and more challenging terminal alkynes were successfully employed for the annulation in good to excellent yield with high regioselectivity.

Chemoselective synthesis of carbamates using CO2 as carbon source

Riemer, Daniel,Hirapara, Pradipbhai,Das, Shoubhik

, p. 1916 - 1920 (2018/08/17)

Synthesis of carbamates directly from amines using CO2 as the carbon source is a straightforward and sustainable approach. Herein, we describe a highly effective and chemoselective methodology for the synthesis of carbamates at room temperature and atmosp

Palladium-catalyzed intramolecular reductive cross-coupling of Csp 2-Csp3 bond formation

Liu, Hui,Wei, Jianpeng,Qiao, Zongjun,Fu, Yana,Jiang, Xuefeng

supporting information, p. 8308 - 8313 (2014/07/08)

A Pd-catalyzed efficient reductive cross-coupling reaction without metallic reductant to construct a Csp2-Csp3 bond has been reported. A PdIV complex was proposed to be a key intermediate, which subsequently went through d

ALLOSTERIC BINDING COMPOUNDS

-

Page/Page column 25-26, (2012/04/23)

The present invention relates to allosteric binding compounds of formula (I), especially for the treatment of CNS disorders, together with pharmaceutical compositions and methods of treatment including these compounds.

INHIBITION OF BACTERIAL BIOFILMS WITH ARYL CARBAMATES

-

Page/Page column 33, (2012/02/01)

Disclosure is provided for carbamate compounds that prevent, remove and/or inhibit the formation of biofilms, compositions including these compounds, devices including these compounds, and methods of using the same.

ALLOSTERIC BINDING COMPOUNDS

-

Page/Page column 69, (2010/09/17)

The present invention relates to allosteric binding compounds of formula (I), especially for the treatment of CNS disorders, together with pharmaceutical compositions and methods of treatment including these compounds.

Mild and selective deprotection of carbamates with Bu4NF

Jacquemard, Ulrich,Bénéteau, Valérie,Lefoix, Myriam,Routier, Sylvain,Mérour, Jean-Yves,Coudert, Gérard

, p. 10039 - 10047 (2007/10/03)

A new mild method allowing the removal of carbamates using TBAF in THF is reported. Reactions were performed on indole, indoline, N-methyl aniline, aniline and tryptamine derivatives. The observed selectivity according to the carbamates or the substrates is discussed. A mechanism is postulated. Graphical Abstract

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