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1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-methoxy-1-[[2-(trimethylsilyl)ethoxy]methyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

290332-98-8

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290332-98-8 Usage

Molecular structure

1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-methoxy-1-[[2-(trimethylsilyl)ethoxy]methyl]-, ethyl ester is a complex organic compound with a pyrrolopyridine core, a carboxylic acid group at one end, and a 4-methoxy-1-[[2-(trimethylsilyl)ethoxy]methyl] group at the other end, connected to an ethyl ester moiety.

Core structure

The compound has a pyrrolopyridine core, which consists of a fusion of a pyrrole and a pyridine ring, providing a stable and rigid structure.

Carboxylic acid group

The presence of a carboxylic acid group (-COOH) at one end of the molecule allows for hydrogen bonding and potential interactions with biological targets, which may be relevant in pharmaceutical applications.

4-Methoxy substitution

The presence of a 4-methoxy group (-OCH3) on the pyridine ring can influence the electronic properties of the molecule and modulate its biological activity.

Trimethylsilyl group

The 2-(trimethylsilyl)ethoxy group serves as a protective group for the molecule, which can be useful in organic synthesis and can be removed under specific conditions to reveal a reactive hydroxyl group.

Ethyl ester moiety

The ethyl ester group (-COOEt) provides an additional site for chemical reactions and can be hydrolyzed to yield the corresponding carboxylic acid.

Potential applications

1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-methoxy-1-[[2-(trimethylsilyl)ethoxy]methyl]-, ethyl ester may have applications in pharmaceutical research due to the presence of a pyridine ring, which is a common structural motif in many drugs. The trimethylsilyl group can also serve as a protective group in organic synthesis, while the carboxylic acid and ester groups provide potential sites for chemical reactions.

Utility in drug discovery and synthetic chemistry

The compound's unique structure and functional groups make it a promising candidate for further exploration in drug discovery and synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 290332-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 290332-98:
(8*2)+(7*9)+(6*0)+(5*3)+(4*3)+(3*2)+(2*9)+(1*8)=138
138 % 10 = 8
So 290332-98-8 is a valid CAS Registry Number.

290332-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-methoxy-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2 ,3-b]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names N-(2-trimethylsilyl)ethoxymethyl-2-ethoxycarbonyl-4-methoxypyrrolo[2,3-b]pyridine

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:290332-98-8 SDS

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