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The chemical compound "4-[hydroxy(2-methylimidazo[1,2-a]pyridin-3-yl)methylidene]-1-(2-methoxyethyl)-5-(4-propoxyphenyl)pyrrolidine-2,3-dione" is a complex organic molecule with a molecular formula of C23H26N2O6. It features a pyrrolidine-2,3-dione core, which is a heterocyclic ring system containing two carbonyl groups. The compound has a 2-methylimidazo[1,2-a]pyridin-3-yl group attached to the 4-position of the pyrrolidine, which contributes to its structure and potential biological activity. Additionally, it has a hydroxy group and a 2-methoxyethyl group at the 1-position, and a 4-propoxyphenyl group at the 5-position, which further modify its chemical properties and interactions. 4-[hydroxy(2-methylimidazo[1,2-a]pyridin-3-yl)methylidene]-1-(2-methoxyethyl)-5-(4-propoxyphenyl)pyrrolidine-2,3-dione is likely to be of interest in pharmaceutical or chemical research due to its intricate structure and potential applications in various fields.

7068-05-5

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7068-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7068-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7068-05:
(6*7)+(5*0)+(4*6)+(3*8)+(2*0)+(1*5)=95
95 % 10 = 5
So 7068-05-5 is a valid CAS Registry Number.

7068-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[hydroxy-(2-methylimidazo[1,2-a]pyridin-3-yl)methylidene]-1-(2-methoxyethyl)-5-(4-propoxyphenyl)pyrrolidine-2,3-dione

1.2 Other means of identification

Product number -
Other names 4-[hydroxy-(8-methyl-1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-9-yl)methylidene]-1-(2-methoxyethyl)-5-(4-propoxyphenyl)pyrrolidine-2,3-dione

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:7068-05-5 SDS

7068-05-5Downstream Products

7068-05-5Relevant academic research and scientific papers

The Cyclopropane-Mediated Ring-Expansion of Propellenes. A New Route to <5.3.1)Propelladienes

Banwell, Martin G.

, p. 1037 - 1049 (2007/10/02)

The propelladiene (1) has been synthesized in six steps from the readily avalaible propellene (10a).Epoxidation of (10a) gives oxide (11a) which undergoes base-promoted rearrangement to allylic alcohol (12a).Simmons-Smith cyclopropanation of (12a) then gives the tetracyclic alcohol (13a).Mild thermolysis of the derived mesylate (14a) affords the ring-expanded isomer (20) which reacts with 1,8-diazabicycloundec-7-ene to give diene (1).A similar sequence of reactions has been used in the preparation of dienol (2) from acetal (10b).Compounds (1) and (2) react with 4-phenyl-4H-1,2,4-triazoline-3,5-dione to give the Diels-Alder adducts (29a) and (29b) respectively.

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