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133427-00-6

IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133427-00-6 Structure

  • Basic information

    1. Product Name: IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester
    2. Synonyms: IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester;ethyl 2-methylimidazo[1,2-a]pyridine-8-carboxylate
    3. CAS NO:133427-00-6
    4. Molecular Formula: C11H12N2O2
    5. Molecular Weight: 204.22518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133427-00-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester(133427-00-6)
    11. EPA Substance Registry System: IMidazo[1,2-a]pyridine-8-carboxylic acid, 2-Methyl-, ethyl ester(133427-00-6)

  • 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: 133427-00-6(Hazardous Substances Data)

133427-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133427-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,2 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133427-00:
(8*1)+(7*3)+(6*3)+(5*4)+(4*2)+(3*7)+(2*0)+(1*0)=96
96 % 10 = 6
So 133427-00-6 is a valid CAS Registry Number.

133427-00-6SDS

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 2-methylimidazo[1,2-a]pyridine-8-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Methyl-imidazo[1,2-a]pyridine-8-carboxylic acid ethyl ester

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:133427-00-6 SDS

133427-00-6Relevant articles and documents

IMIDAZO [1, 2-A] PYRROLO [3, 2-C] PYRIDINE COMPOUNDS USEFUL AS PESTIVIRUS INHIBITORS

-

Page/Page column 18, (2010/04/30)

The present invention relates to a series of novel imidazo[1,2-α]pyrrolo[3,2-c]pyridines (or also named 6H-1,3a,6-Tri-aza-αy-indacenes) and derivatives thereof, according to formula: (I); The present invention also relates to processes for the preparation of imidazo[1,2-α]pyrrolo[3,2-c]pyridines, their use as. a, medicine, their use to treat or prevent viral infections and their use to manufacture a medicine to treat or prevent viral infections, particularly infections with viruses belonging to the family of the Flaviviridae and more preferably infections with Bovine Viral Diarrhea virus (BVDV).

Synthesis and antiviral activity of an imidazo[1,2-a]pyrrolo[2,3-c]pyridine series against the bovine viral diarrhea virus

Chezal, Jean-Michel,Paeshuyse, Jan,Gaumet, Vincent,Canitrot, Damien,Maisonial, Aurélie,Lartigue, Claire,Gueiffier, Alain,Moreau, Emmanuel,Teulade, Jean-Claude,Chavignon, Olivier,Neyts, Johan

supporting information; experimental part, p. 2044 - 2047 (2010/06/20)

A series of imidazo[1,2-a]pyrrolo[2,3-c]pyridines has been prepared and evaluated for their anti-BVDV activities in MDBK cells. From the synthesized analogues bearing modifications of the substituents at positions 2, 3, 7 and 8, compounds 10a, b, 16, 24, 25 and 26 exhibited significant anti-BVDV activities.

New opportunities with the Duff reaction

Masurier, Nicolas,Moreau, Emmanuel,Lartigue, Claire,Gaumet, Vincent,Chezal, Jean-Michel,Heitz, Annie,Teulade, Jean-Claude,Chavignon, Olivier

, p. 5989 - 5992 (2008/12/21)

(Chemical Equation Presented) The Duff reaction (HMTA, AcOH or TFA) was studied on substituted [6 + 5] heterocyclic compounds. This reaction provides a useful route to aldehydes for compounds bearing sensitive amide functions. It gives also access to tric

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