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6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is a chemical compound belonging to the imidazo[1,2-a]pyridine class. It is an ethyl ester derivative of 6-bromo-2-phenylimidazo[1,2-a]pyridine-3-carboxylic acid, which exhibits potential antineoplastic activity. This unique structure and properties make it a promising candidate for further research and development in the field of medicinal chemistry, particularly for the treatment of cancer and other diseases.

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  • 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER

    Cas No: 885276-79-9

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  • 885276-79-9 Structure
  • Basic information

    1. Product Name: 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER
    2. Synonyms: 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER;Imidazo[1,2-a]pyridine-3-carboxylic acid, 6-bromo-2-phenyl-, ethyl ester
    3. CAS NO:885276-79-9
    4. Molecular Formula: C16H13BrN2O2
    5. Molecular Weight: 345.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885276-79-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.46g/cm3
    6. Refractive Index: 1.643
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER(885276-79-9)
    11. EPA Substance Registry System: 6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER(885276-79-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 885276-79-9(Hazardous Substances Data)

885276-79-9 Usage

Uses

Used in Pharmaceutical Industry:
6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a potential antineoplastic agent for the development of new drugs to treat cancer. Its unique structure and properties make it a promising candidate for further research and development in the field of medicinal chemistry.
Used in Medicinal Chemistry Research:
6-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a subject of study for understanding its potential applications in the development of new drugs and therapies. Its unique structure and properties contribute to the advancement of knowledge in medicinal chemistry and the discovery of novel treatments for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 885276-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885276-79:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*6)+(2*7)+(1*9)=229
229 % 10 = 9
So 885276-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H13BrN2O2/c1-2-21-16(20)15-14(11-6-4-3-5-7-11)18-13-9-8-12(17)10-19(13)15/h3-10H,2H2,1H3

885276-79-9SDS

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 6-bromo-2-phenylimidazo[1,2-a]pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names S14-2123

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:885276-79-9 SDS

885276-79-9Downstream Products

885276-79-9Relevant articles and documents

Thermal and microwave-assisted rapid syntheses of substituted imidazo[1,2-a]pyridines under solvent- and catalyst-free conditions

Chunavala, Kaushik C.,Joshi, Girdhar,Suresh, Eringathodi,Adimurthy, Subbarayappa

experimental part, p. 635 - 641 (2011/04/15)

Thermal and microwave-assisted rapid syntheses of highly substituted imidazo[1,2-a]pyridine derivatives by reaction of aminopyridines and -bromo - keto esters under solvent-free conditions are described. Reactions carried out under microwave irradiation give the highest yields of products in reaction times of less than two minutes. Georg Thieme Verlag Stuttgart New York.

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