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5H-Imidazo[2,1-a]isoindol-5-one, 2,3-dihydro- is a chemical compound with the molecular formula C9H7N. It belongs to the class of imidazoisoindolones, which are heterocyclic compounds containing both imidazole and isoindole rings. This specific compound is characterized by the presence of a 5-membered imidazole ring fused to a 5-membered isoindole ring, with a carbonyl group at the 5-position and a double bond between the 2 and 3 positions. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential antitumor, antiviral, and anti-inflammatory properties. The compound is also known for its ability to modulate the activity of certain enzymes and receptors, making it a valuable tool in medicinal chemistry research.

16780-94-2

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16780-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16780-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,8 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16780-94:
(7*1)+(6*6)+(5*7)+(4*8)+(3*0)+(2*9)+(1*4)=132
132 % 10 = 2
So 16780-94-2 is a valid CAS Registry Number.

16780-94-2SDS

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 2,3-dihydro-imidazo[2,1-a]isoindol-5-one

1.2 Other means of identification

Product number -
Other names 2,3-Dihydro-imidazo[2,1-a]isoindol-5-on

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

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More Details:16780-94-2 SDS

16780-94-2Downstream Products

16780-94-2Relevant academic research and scientific papers

The Reactivity of Imide Carbnyl Groups in the Intramolecular Aza-Wittig Reaction. An Efficient Route to Iminolactam Derivatives

Eguchi, Shoji,Takeuchi, Hisato

, p. 602 - 603 (2007/10/02)

Treatment of N-(ω-azidoalkyl)imides with triphenylphosphine in toluene or xylene under reflux gave the corresponding iminolactam derivatives in good yields via Staudinger reaction followed by the intramolecular aza-Wittig reaction.

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