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80212-88-0

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80212-88-0 Usage

Chemical structure

Contains a piperidine ring and a triazole ring, with a cyclopropyl group and a nitrophenyl group attached to the triazole ring.

Application in medicinal chemistry

Potential antipsychotic drug.

Receptor activity

Exhibits antagonistic activity at dopamine D2 and serotonin 5-HT2A receptors.

Neurodegenerative diseases

Studied for potential use in treating Alzheimer's disease.

Antimicrobial properties

Investigated for its potential as an antimicrobial agent.

Anti-inflammatory properties

Investigated for its potential as an anti-inflammatory agent.

Versatility

Potential applications in various fields due to its multiple properties.

Check Digit Verification of cas no

The CAS Registry Mumber 80212-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,1 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80212-88:
(7*8)+(6*0)+(5*2)+(4*1)+(3*2)+(2*8)+(1*8)=100
100 % 10 = 0
So 80212-88-0 is a valid CAS Registry Number.

80212-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-cyclopropyl-5-(4-nitrophenyl)triazol-4-yl]piperidine

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:80212-88-0 SDS

80212-88-0Upstream product

80212-88-0Downstream Products

80212-88-0Relevant articles and documents

Syntheses with Alkenediazonium Salts, II. On the Synthesis of 4-(4-Nitrophenyl)-5-piperidino-1H-1,2,3-triazoles from 2-Ethoxy-1-(4-nitrophenyl)-2-piperidino-1-ethenediazonium Hexachloroantimonate with Primary Amines

Saalfrank, Rolf W.,Ackermann, Erich

, p. 3456 - 3459 (2007/10/02)

Reaction of 2-ethoxy-1-(4-nitrophenyl)-2-piperidino-1-ethenediazonium hexachloroantimonate (1) with primary amines 2 leads to 4-(4-nitrophenyl)-4-piperidino-1H-1,2,3-triazoles 9 in good yields.

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