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199192-18-2

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199192-18-2 Usage

General Description

3-Indolizinecarboxaldehyde, 5,6,7,8-tetrahydro- (9CI) is a chemical compound with the molecular formula C10H11NO. It is an aldehyde derivative of indolizine and is also known as 5,6,7,8-tetrahydro-3H-indolizin-3-carbaldehyde. 3-Indolizinecarboxaldehyde, 5,6,7,8-tetrahydro- (9CI) is used in the synthesis of various organic compounds and has potential applications in medicinal chemistry and drug development. It has been studied for its potential biological activities and may have promising pharmacological properties. However, further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 199192-18-2 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, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 199192-18:
(8*1)+(7*9)+(6*9)+(5*1)+(4*9)+(3*2)+(2*1)+(1*8)=182
182 % 10 = 2
So 199192-18-2 is a valid CAS Registry Number.

199192-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8-tetrahydroindolizine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-Indolizinecarboxaldehyde,5,6,7,8-tetrahydro

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:199192-18-2 SDS

199192-18-2Upstream product

199192-18-2Downstream Products

199192-18-2Relevant articles and documents

Bu3SnH-mediated radical cyclisation onto azoles

Allin, Steven M.,Barton, William R.S.,Russell Bowman,Bridge (née Mann), Emma,Elsegood, Mark R.J.,McInally, Tom,McKee, Vickie

, p. 7745 - 7758 (2008/12/21)

Alkyl radicals have been cyclised onto pyrroles, imidazoles and pyrazoles, and acyl radicals cyclised onto pyrroles, using Bu3SnH-, (TMS)3SiH- and Bu3GeH-mediated aromatic homolytic substitution for the synthesis of bicyclic N-heterocycles. The reactions yield intermediate π-radicals that lose hydrogen in the?rearomatisation step of the aromatic homolytic substitution. Mechanistic studies of these rearomatisation steps indicate aromatic homolytic substitution in which the initiator or breakdown products from the inhibitor are responsible for the H-abstraction step.

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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