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199192-25-1

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199192-25-1 Usage

Chemical group

Imidazole derivatives

Physical appearance

White to yellow solid substance

Odor

Pungent

Main use

Raw material for production of pharmaceuticals and agricultural chemicals

Chemical structure

Contains a propyl group attached to the imidazole ring

Effect of propyl group

Affects properties and reactivity

Potential applications

Building block for synthesis of various compounds

Check Digit Verification of cas no

The CAS Registry Mumber 199192-25-1 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 199192-25:
(8*1)+(7*9)+(6*9)+(5*1)+(4*9)+(3*2)+(2*2)+(1*5)=181
181 % 10 = 1
So 199192-25-1 is a valid CAS Registry Number.

199192-25-1SDS

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 1H-Imidazole-5-carboxaldehyde,1-propyl-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:199192-25-1 SDS

199192-25-1Downstream Products

199192-25-1Relevant articles and documents

Identification of novel imidazole flavonoids as potent and selective inhibitors of protein tyrosine phosphatase

Zhang, Ling,Ge, Yu,Wang, Qing Ming,Zhou, Cheng-He

, (2019/04/17)

A series of imidazole flavonoids as new type of protein tyrosine phosphatase inhibitors were synthesized and characterized. Most of them gave potent protein phosphatase 1B (PTP1B) inhibitory activities. Especially, compound 11a could effectively inhibit P

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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