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5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE is a heterocyclic aromatic aldehyde with the molecular formula C8H6FN3O. It is a yellow solid that features a fluorine atom, an imidazole ring, and a pyridine ring in its structure. This chemical compound is recognized for its versatility in organic synthesis and serves as a valuable building block in the creation of pharmaceuticals and agrochemicals.

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  • 878197-67-2 Structure
  • Basic information

    1. Product Name: 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE
    2. Synonyms: 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE;5-Fluoroimidazo[1,2-a]pyridine-2-carbaldehyde;5-Fluoro-2-formylimidazo[1,2-a]pyridine
    3. CAS NO:878197-67-2
    4. Molecular Formula: C8H5FN2O
    5. Molecular Weight: 164.139
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 878197-67-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.369 g/cm3
    6. Refractive Index: 1.618
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE(878197-67-2)
    11. EPA Substance Registry System: 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE(878197-67-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 878197-67-2(Hazardous Substances Data)

878197-67-2 Usage

Uses

Used in Pharmaceutical Industry:
5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs, enhancing the therapeutic potential of medications in treating diverse health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE is utilized as a vital component in the production of agrochemicals. Its incorporation aids in the development of effective pesticides and other agricultural chemicals, thereby supporting crop protection and yield enhancement.
Used in Organic Synthesis:
5-FLUOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXALDEHYDE is employed as a versatile building block in organic synthesis. Its distinctive structure allows for the creation of a wide range of chemical products, expanding the scope of chemical research and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 878197-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,1,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 878197-67:
(8*8)+(7*7)+(6*8)+(5*1)+(4*9)+(3*7)+(2*6)+(1*7)=242
242 % 10 = 2
So 878197-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H5FN2O/c9-7-2-1-3-8-10-6(5-12)4-11(7)8/h1-5H

878197-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoroimidazo[1,2-a]pyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-fluoroimidazo[1,2-a]pyridine-2-carbaldehyde

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:878197-67-2 SDS

878197-67-2Relevant articles and documents

Imidazopyridine-5,6,7,8-tetrahydro-8-quinolinamine derivatives with potent activity against HIV-1

Gudmundsson, Kristjan S.,Boggs, Sharon D.,Catalano, John G.,Svolto, Angilique,Spaltenstein, Andrew,Thomson, Michael,Wheelan, Pat,Jenkinson, Stephen

scheme or table, p. 6399 - 6403 (2010/05/02)

Synthesis of several novel imidazopyridine-5,6,7,8-tetrahydro-8-quinolinamine derivatives with potent activity against HIV are described. Synthetic approaches allowing for variation of the substitution pattern are outlined and resulting changes in antivir

Kilogram-scale synthesis of the CXCR4 antagonist GSK812397

Boggs, Sharon,Elitzin, Vassil I.,Gudmundsson, Kristjan,Martin, Michael T.,Sharp, Matthew J.

scheme or table, p. 781 - 785 (2010/04/22)

An improved, scalable synthesis of the CXCR4 antagonist GSK812397 is described. This new route was recently scaled up in 50 L fixed equipment to afford 1.2 kg of drug substance in five steps with an overall yield of 20% and >99% chemical and enantiomeric

CHEMICAL COMPOUNDS

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Page/Page column 35-36, (2008/06/13)

The present invention provides compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind to chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 of a

CHEMICAL COMPOUNDS

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Page/Page column 44-45; 59-60, (2010/11/28)

The present invention provides compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind to chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 of a

CHEMICAL COMPOUNDS

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Page/Page column 40-41, (2008/06/13)

There is provided novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as C

CHEMCIAL COMPOUNDS

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Page/Page column 60-61, (2010/10/20)

The present invention provides novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 and/or CCR5 of a target cell.

CHEMICAL COMPOUNDS

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Page/Page column 65, (2010/11/08)

The present invention provides novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a recep

CHEMICAL COMPOUNDS

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Page/Page column 44-45, (2008/06/13)

The present invention provides compounds of Formula (I) comprising: including salts, solvates, and physiologically functional derivatives thereof, pharmaceutical formulations containing them, processes for their preparation, and methods of treatment using them.

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