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Imidazo[1,2-a]pyridine-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199192-27-3 Structure
  • Basic information

    1. Product Name: Imidazo[1,2-a]pyridine-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI)
    2. Synonyms: Imidazo[1,2-a]pyridine-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI)
    3. CAS NO:199192-27-3
    4. Molecular Formula: C8H10N2O
    5. Molecular Weight: 150.1778
    6. EINECS: N/A
    7. Product Categories: ALDEHYDE;AMINETERTIARY
    8. Mol File: 199192-27-3.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-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Imidazo[1,2-a]pyridine-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI)(199192-27-3)
    11. EPA Substance Registry System: Imidazo[1,2-a]pyridine-3-carboxaldehyde, 5,6,7,8-tetrahydro- (9CI)(199192-27-3)
  • 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: 199192-27-3(Hazardous Substances Data)

199192-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199192-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,1,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199192-27:
(8*1)+(7*9)+(6*9)+(5*1)+(4*9)+(3*2)+(2*2)+(1*7)=183
183 % 10 = 3
So 199192-27-3 is a valid CAS Registry Number.

199192-27-3SDS

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 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-formyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

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:199192-27-3 SDS

199192-27-3Downstream Products

199192-27-3Relevant articles and documents

Synthesis, biological evaluation and molecular modelling of sulfonohydrazides as selective PI3K p110α inhibitors

Kendall, Jackie D.,Rewcastle, Gordon W.,Frederick, Raphael,Mawson, Claire,Denny, William A.,Marshall, Elaine S.,Baguley, Bruce C.,Chaussade, Claire,Jackson, Shaun P.,Shepherd, Peter R.

, p. 7677 - 7687 (2008/03/14)

A series of 2-methyl-5-nitrobenzenesulfonohydrazides were prepared and evaluated as inhibitors of PI3K. An isoquinoline derivative shows good selectivity for the p110α isoform over p110β and p110δ, and also demonstrates good in vitro activity in a cell pr

3-‘4-HETEROCYCLYL -1,2,3,-TRIAZOL-1-YL!-N-ARYL-BENZAMIDES AS INHIBITORS OF THE CYTOKINES PRODUCTION FOR THE TREATMENT OF CHRONIC INFLAMMATORY DISEASES

-

Page/Page column 98, (2008/06/13)

Disclosed compounds of formula (I), which inhibit production of cytokines involved in inflammatory processes and are thus useful for treating diseases and pathological conditions involving inflammation such as chronic inflammatory disease. Also disclosed are processes for preparing these compounds and pharmaceutical compositions comprising these compounds.

BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

-

Page 239, (2010/02/06)

The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.

Bu3SnH mediated oxidative radical cyclisation onto imidazoles and pyrroles

Aldabbagh, Fawaz,Russell Bowman,Mann, Emma,Slawin, Alexandra M.Z.

, p. 8111 - 8128 (2007/10/03)

A new protocol using radical cyclisation has been developed for the synthesis of [1,2-c]-fused imidazoles and [1,2-a]-fused pyrroles. The intermediate nucleophilic N-alkyl radicals, generated using Bu3SnH from N- (ω-bromoalkyl) or N-[ω-(phenylselanyl)alkyl] imidazoles and pyrroles, undergo regio-selective radical cyclisalion onto the azole rings followed by oxidative re-aromatisation.

Oxidative radical cyclisations onto imidazoles and pyrroles using Bu3SnH

Aldabbagh, Fawaz,Bowman, W. Russell,Mann, Emma

, p. 7937 - 7940 (2007/10/03)

Oxidative radical cyclisation using Bu3SnH has been used for the synthesis of [1,2-c]-fused imidazoles and [1,2-a]-fused pyrroles from imidazolecarbaldehydes and acylpyrroles respectively. The intermediate nucleophilic N-alkyl radicals cyclise onto imidazole and pyrrole rings followed by oxidative re-aromatisation.

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