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1,5-dihydro-7-(1-piperidinyl)-imidazo(2,1-b)quinazolin-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96086-67-8

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96086-67-8 Usage

Molecular structure

The compound has a complex molecular structure consisting of a quinazolin-2(3H)-one core with a piperidinyl substituent at the 7th position and a dihydro-1,5 arrangement.

Chemical family

It belongs to the imidazoquinazolinone family, which is a group of chemical compounds with potential pharmacological properties.

Pharmacological interest

The compound is of interest due to its potential pharmacological properties, which may lead to applications in drug discovery and development.

Medicinal chemistry

It may be useful in the field of medicinal chemistry for the design of novel therapeutic agents, given its unique structural features and potential pharmacological properties.

Biological activities

The compound's structural features may make it suitable for studying various biological activities and interactions within the human body.

Further research

More research is needed to fully understand the chemical and biological properties of 1,5-dihydro-7-(1-piperidinyl)-imidazo(2,1-b)quinazolin-2(3H)-one, as its potential applications and interactions are not yet fully known.

Potential applications

Given its pharmacological interest and potential for studying biological activities, the compound may have applications in the development of new drugs and therapeutic agents.

Synthesis methods

The synthesis of 1,5-dihydro-7-(1-piperidinyl)-imidazo(2,1-b)quinazolin-2(3H)-one may involve complex chemical reactions and techniques, which could be optimized for large-scale production or further modification of the compound.

Safety and toxicity

As with any new compound, it is essential to evaluate the safety and potential toxicity of 1,5-dihydro-7-(1-piperidinyl)-imidazo(2,1-b)quinazolin-2(3H)-one before considering its use in drug development or therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 96086-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,8 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96086-67:
(7*9)+(6*6)+(5*0)+(4*8)+(3*6)+(2*6)+(1*7)=168
168 % 10 = 8
So 96086-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N4O.2ClH/c20-14-10-19-9-11-8-12(18-6-2-1-3-7-18)4-5-13(11)16-15(19)17-14;;/h4-5,8H,1-3,6-7,9-10H2,(H,16,17,20);2*1H

96086-67-8SDS

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 7-piperidino-1,2,3,5-tetrahydroimidazo[2,1-b]-quinazolin-2-one

1.2 Other means of identification

Product number -
Other names 7-piperidino-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-one

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:96086-67-8 SDS

96086-67-8Downstream Products

96086-67-8Relevant academic research and scientific papers

7-piperidino-1,2,3,5-tetrahydroimidazo[2,1-b]-quinazolin-2-one having platelet aggregation inhibitory activity

-

, (2008/06/13)

7-Piperidino-1,2,3,5-tetrahydroimidazo[2,1-b]-quinazolin-2-one having platelet aggregation inhibitory activity is disclosed. The compound has high water-solubility and reduced influences on the circulatory system.

Cyclic guanidines. 17. Novel (N-substituted amino)imidazo[2,1-b]quinazolin-2-ones: Water-soluble platelet aggregation inhibitors

Ishikawa,Saegusa,Inamura,Sakuma,Ashida

, p. 1387 - 1393 (2007/10/02)

A series of novel 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-one derivatives substituted with a secondary amino group has been prepared and tested for the activities of inhibiting platelet aggregation in rats in vitro and ex vivo. Most of the compounds

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