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Ethyl 2-[3-(ethoxycarbonylmethyl)-1-methyl-2-oxo-indol-3-yl]acetate is a complex organic compound with the molecular formula C18H19NO5. It is a derivative of indole, a heterocyclic aromatic organic compound, and features an ethyl ester group attached to the acetate moiety. ethyl 2-[3-(ethoxycarbonylmethyl)-1-methyl-2-oxo-indol-3-yl]acetate is characterized by a 3-(ethoxycarbonylmethyl)-1-methyl-2-oxo-indol-3-yl group, which is a modified indole structure with an ethoxycarbonylmethyl group and a methyl group attached to the nitrogen atom. The compound has potential applications in pharmaceuticals and chemical research due to its unique structure and properties.

7145-09-7

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7145-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7145-09-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7145-09:
(6*7)+(5*1)+(4*4)+(3*5)+(2*0)+(1*9)=87
87 % 10 = 7
So 7145-09-7 is a valid CAS Registry Number.

7145-09-7SDS

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-[3-(2-ethoxy-2-oxoethyl)-1-methyl-2-oxoindol-3-yl]acetate

1.2 Other means of identification

Product number -
Other names 3H-Indole-3,3-diacetic acid,1,2-dihydro-1-methyl-2-oxo-,diethyl 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:7145-09-7 SDS

7145-09-7Downstream Products

7145-09-7Relevant academic research and scientific papers

N-hydroxyalkyl derivatives of 3β-phenyltropane and 1-methylspiro[1H- indoline-3,4'-piperidine]: Vesamicol analogues with affinity for monoamine transporters

Efange, Simon M. N.,Kamath, Ashok P.,Khare, Anil B.,Kung, Mei-Ping,Mach, Robert H.,Parsons, Stanley M.

, p. 3905 - 3914 (2007/10/03)

As part of our ongoing structure-activity studies of the vesicular acetylcholine transporter ligand 2-(4-phenylpiperidino)cyclohexanol [vesamicol, 1), 22 N-hydroxy(phenyl)alkyl derivatives of 3β-phenyltropane, 6, and 1-methylspiro[1H-indoline-3,4'-piperidine], 7, were synthesized and tested for binding in vitro. Although a few compounds displayed moderately high affinity for the vesicular acetylcholine transporter, no compound was more potent than the prototypical vesicular acetylcholine transporter ligand vesamicol. However, a few derivatives of 6 displayed higher affinity for the dopamine transporter than cocaine. We conclude that modification of the piperidyl fragment of 1 will not lead to more potent vesicular acetylcholine transporter ligands.

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