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1H-Indole-2-carboxylic acid, 5-chloro-6-fluoro-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

473257-60-2

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473257-60-2 Usage

Indole Derivative

The compound belongs to the family of indole derivatives, which are organic compounds that contain a bicyclic structure with a benzene ring and a pyrrole ring.

Organic Ester

The compound is an organic ester, which is a type of organic compound that contains an ester group (R-COO-R') formed by the reaction of an acid and an alcohol.

Indole Ring

The compound is characterized by the presence of an indole ring, which is a bicyclic structure with a benzene ring and a pyrrole ring.

Carboxylic Acid Group

The compound contains a carboxylic acid group (-COOH), which is a functional group that consists of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom.

Chloro and Fluoro Substituents

The compound has chloro (-Cl) and fluoro (-F) substituents at specific positions within the indole ring, which are halogens that can affect the compound's reactivity and properties.

Ethyl Ester

The compound is an ethyl ester, which is an ester formed by the reaction of an acid with ethanol (C2H5OH).

Applications in Organic Synthesis

The compound has applications in organic synthesis, which is the process of creating new compounds by chemically bonding atoms or molecules together.

Pharmaceutical Applications

The compound has applications in pharmaceuticals, which are substances used in the treatment, cure, prevention, or diagnosis of diseases.

New Material Development

The compound is used in the development of new materials, which are substances or products that are created to meet specific needs or functions.

Building Block in Chemical Compound Creation

The compound is utilized as a building block in the creation of various chemical compounds and products, which means it can be used as a starting material in the synthesis of other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 473257-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,2,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 473257-60:
(8*4)+(7*7)+(6*3)+(5*2)+(4*5)+(3*7)+(2*6)+(1*0)=162
162 % 10 = 2
So 473257-60-2 is a valid CAS Registry Number.

473257-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate

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:473257-60-2 SDS

473257-60-2Downstream Products

473257-60-2Relevant academic research and scientific papers

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

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Paragraph 00287, (2017/09/27)

The present invention provides compounds, compositions thereof, and methods of using the same.

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

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Paragraph 00265, (2017/10/06)

The present invention provides compounds, compositions thereof, and methods of using the same.

SUBSTITUTED INDOLE COMPOUND

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Page/Page column 187-188, (2010/11/24)

Disclosed is an excellent LXR modulator. A compound represented by the general formula (I): (I) wherein R1, R2, R3 and R4: H, an alkyl which may be substituted, OH, an alkoxy which may be substituted, an amino which may be substituted, a halogeno, a phenyl or the like; R5: H or an alkyl; R6: -COR8 (wherein R8: an alkoxy which may be substituted, a phenyloxy which may be substituted, an amino which may be substituted, or the like), -SO2R9 (wherein R9: an alkyl which may be substituted, a phenyl which may be substituted or a heterocyclyl which may be substituted), or an alkyl which may be substituted; R7: -X2R10 [wherein R10: -COR11 (where R11: OH, an alkoxy which may be substituted or an amino which may be substituted), -SO2R12 (where R12: an alkyl which may be substituted or amino which may be substituted), -N(R13)COR14 (where R13: H or an alkyl which may be substituted; R14: H or an alkyl which may be substituted), -N(R13)SO2R15 (where R13: as defined above; R15: an alkyl which may be substituted) or tetrazol-5-yl; and X2: a single bond or an alkylene which may be substituted]; X1: a methylene which may be substituted; Y1: a phenyl which may be substituted or a heterocyclyl which may be substituted; and Y2: an aryl which may be substituted, a heterocyclyl which may be substituted or the like], or the like.

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