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2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE] is a unique spiro compound characterized by an indene ring fused to a piperidine ring. It belongs to the spiro compound family and holds potential pharmacological importance due to its diverse biological activities, including antipsychotic, analgesic, and anti-inflammatory properties. 2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE] has been studied for its potential use in treating various neurological and psychiatric disorders, and its distinctive spiro structure makes it an intriguing target for synthetic and medicinal chemistry research, offering opportunities for developing novel drugs with enhanced therapeutic profiles.

428-38-6

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428-38-6 Usage

Uses

Used in Pharmaceutical Industry:
2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE] is used as a pharmaceutical agent for its potential role in the treatment of neurological and psychiatric disorders. Its antipsychotic, analgesic, and anti-inflammatory properties make it a promising candidate for further research and development in this field.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,3-DIHYDROSPIRO[INDENE-1,4'-PIPERIDINE] is utilized as a subject of study for its unique spiro ring system. Researchers are interested in exploring its structure for the development of novel drugs with improved therapeutic profiles, leveraging its diverse biological activities for innovative pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 428-38-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 428-38:
(5*4)+(4*2)+(3*8)+(2*3)+(1*8)=66
66 % 10 = 6
So 428-38-6 is a valid CAS Registry Number.

428-38-6SDS

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 spiro[1,2-dihydroindene-3,4'-piperidine]

1.2 Other means of identification

Product number -
Other names spiroindane

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:428-38-6 SDS

428-38-6Relevant academic research and scientific papers

INDOL-3-YL-CARBONYL-SPIRO-PIPERIDINE DERIVATIVES AS V1A RECEPTOR ANTAGONISTS

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Page/Page column 35-36, (2008/06/13)

The invention relates to indol-3-yl-carbonyl-spiro-piperidine derivatives which act as V1a receptor antagonists and which are represented by Formula I: wherein the spiro-piperidine head group A and the residues R1, R2 and R3 are as defined herein. The invention further relates to pharmaceutical compositions containing such compounds, methods for preparing the compounds and pharmaceutical compositions, and their use in the treatment of dysmenorrhea, hypertension, chronic heart failure, inappropriate secretion of vasopressin, liver cirrhosis, nephrotic syndrome, obsessive compulsive disorder, anxious and depressive disorders.

CARBOXYAMINE COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 72, (2010/11/26)

The invention relates to the use of carboxyamine compounds and salts thereof in the treatment of HDAC dependent diseases and for the manufacture of pharmaceutical preparations for the treatment of said diseases.

Synthesis and biological activities of spiroheterocyclic growth hormone secretagogues

Chen, Meng-Hsin,Pollard, Patrick P.,Patchett, Arthur A.,Cheng, Kang,Liente, Wei,Chan, Wanda W.-S.,Butler, Bridget,Jacks, Thomas M.,Smith, Roy G.

, p. 1261 - 1266 (2007/10/03)

The synthesis and biological activities of a series of spiroheterocyclic growth hormone secretagogues are reported. Modification of the spiroindane part-structure of the prototypal secretagogue L-162,752 revealed that the spiroindane could be replaced with spirobenzodihydrothiophen derivatives to enhance not only in vitro potency but also oral activity. In this study non- aromatic D-2-amino-4-cyclohexylbutanoic analogs (8a-8d) were also identified to be active secretagogues.

SPIROCYCLIC ANTIPSYCHOTIC AGENTS

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, (2008/06/13)

A class of spirocyclic piperidine derivatives are selective ligands at sigma recognition sites and are therefore useful in the treatment and/or prevention of psychiatric disorders.

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