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1353985-76-8

3-benzyl-6-methyl-2-(thiophene-2-yl)imidazo[1,2-a]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1353985-76-8 Structure

  • Basic information

    1. Product Name: 3-benzyl-6-methyl-2-(thiophene-2-yl)imidazo[1,2-a]pyridine
    2. Synonyms:
    3. CAS NO:1353985-76-8
    4. Molecular Formula:
    5. Molecular Weight: 304.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1353985-76-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-benzyl-6-methyl-2-(thiophene-2-yl)imidazo[1,2-a]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzyl-6-methyl-2-(thiophene-2-yl)imidazo[1,2-a]pyridine(1353985-76-8)
    11. EPA Substance Registry System: 3-benzyl-6-methyl-2-(thiophene-2-yl)imidazo[1,2-a]pyridine(1353985-76-8)

  • 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: 1353985-76-8(Hazardous Substances Data)

1353985-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1353985-76-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,9,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1353985-76:
(9*1)+(8*3)+(7*5)+(6*3)+(5*9)+(4*8)+(3*5)+(2*7)+(1*6)=198
198 % 10 = 8
So 1353985-76-8 is a valid CAS Registry Number.

1353985-76-8Downstream Products

1353985-76-8Relevant articles and documents

Synthesis of Imidazo[1,2-a]pyridines using fe3o 4@sio2 as an efficient Nanomagnetic catalyst via a one-pot Multicomponent reaction

Maleki, Ali

, p. 587 - 593 (2014)

A one-pot multicomponent synthesis of imidazo[1,2-a]pyridine derivatives by using pyridin-2-amines, aldehydes, and terminal alkynes in the presence of a catalytic amount of silica-supported iron oxide (Fe3O 4@SiO2) nanopar

Nonacidic Farnesoid X Receptor Modulators

Flesch, Daniel,Cheung, Sun-Yee,Schmidt, Jurema,Gabler, Matthias,Heitel, Pascal,Kramer, Jan,Kaiser, Astrid,Hartmann, Markus,Lindner, Mara,Lüddens-D?mgen, Kerstin,Heering, Jan,Lamers, Christina,Lüddens, Hartmut,Wurglics, Mario,Proschak, Ewgenij,Schubert-Zsilavecz, Manfred,Merk, Daniel

supporting information, p. 7199 - 7205 (2017/09/07)

As a cellular bile acid sensor, farnesoid X receptor (FXR) participates in regulation of bile acid, lipid and glucose homeostasis, and liver protection. Clinical results have validated FXR as therapeutic target in hepatic and metabolic diseases. To date, potent FXR agonists share a negatively ionizable function that might compromise their pharmacokinetic distribution and behavior. Here we report the development and characterization of a high-affinity FXR modulator not comprising an acidic residue.

Mechanistic studies on a new catalyst system (CuI-NaHSO4· SiO2) leading to the one-pot synthesis of imidazo[1,2- a ]pyridines from reactions of 2-aminopyridines, aldehydes, and terminal alkynes

Mishra, Sarita,Ghosh, Rina

experimental part, p. 3463 - 3470 (2011/12/04)

One-pot reactions of aldehydes, 2-aminopyridines, and terminal alkynes, in the presence of the copper(I) iodide-NaHSO4·SiO2 combination catalyst in refluxing toluene, generate the corresponding imidazo[1,2-a]pyridines in high to excellent yields; the mechanism has been studied. Georg Thieme Verlag Stuttgart.

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