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61063-11-4

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61063-11-4 Usage

Uses

2-Amino-3-nitrobenzoic Acid Ethyl Ester, is a building block used in synthesis of various compounds, such as Ethyl 4-[4-(4-Substituted Piperidin-1-yl)]benzylpyrrolo[1,2-a]quinoxalinecarboxylate derivatives having Antiproliferative effect on human leukemia cells.

Check Digit Verification of cas no

The CAS Registry Mumber 61063-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,6 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61063-11:
(7*6)+(6*1)+(5*0)+(4*6)+(3*3)+(2*1)+(1*1)=84
84 % 10 = 4
So 61063-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O4/c1-2-15-9(12)6-4-3-5-7(8(6)10)11(13)14/h3-5H,2,10H2,1H3

61063-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-amino-3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid, 2-amino-3-nitro-, ethyl ester

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:61063-11-4 SDS

61063-11-4Relevant articles and documents

Organic Nanotube with Subnanometer, pH-Responsive Lumen

Darnall, Shawn M.,Li, Changyi,Dunbar, Martha,Alsina, Marco,Keten, Sinan,Helms, Brett A.,Xu, Ting

supporting information, p. 10953 - 10957 (2019/08/07)

While many synthetic nanotubes with a hydrophobic lumen and fast molecular transport have been developed, decorating the interior of these channels with polar and/or responsive functional groups remains challenging. In transmembrane proteins like the aqua

Synthesis and biological evaluation of novel substituted pyrrolo[1,2-a] quinoxaline derivatives as inhibitors of the human protein kinase CK2

Guillon, Jean,Le Borgne, Marc,Rimbault, Charlotte,Moreau, Stéphane,Savrimoutou, Solène,Pinaud, No?l,Baratin, Sophie,Marchivie, Mathieu,Roche, Séverine,Bollacke, Andre,Pecci, Adali,Alvarez, Lautaro,Desplat, Vanessa,Jose, Joachim

, p. 205 - 222 (2013/10/01)

Herein we describe the synthesis and properties of substituted phenylaminopyrrolo[1,2-a]quinoxaline-carboxylic acid derivatives as a novel class of potent inhibitors of the human protein kinase CK2. A set of 15 compounds was designed and synthesized using

IMIDAZO(1,2-a)PYRIDINE DERIVATIVE

-

Page 106; 107, (2010/02/09)

A compound reprsented by the following formula (I), its salts or nsolvates thereof capable of specifically or selectively expressig an antifungal activity in a broad spectrum based on the novel mechanism thereof of 1,6-β-glucan synthesis inhibition, and an antifungal agent containing any of them.

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