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(3-iodobenzyl)trozamicol is a chemical compound derived from the trozamicol family, characterized by the addition of an iodine atom to the benzene ring. This modification endows the compound with unique properties and potential applications in the realms of pharmaceutical research and drug development. As a derivative of trozamicol, a synthetic compound with recognized potential as a cognitive enhancer and memory booster, (3-iodobenzyl)trozamicol shares structural similarities that may confer pharmacological properties. Its synthesis and characterization could offer significant contributions to the development of novel therapeutic agents in cognitive enhancement and neuropharmacology. However, further research is essential to comprehensively understand its potential uses and effects.

148519-95-3

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148519-95-3 Usage

Uses

Used in Pharmaceutical Research:
(3-iodobenzyl)trozamicol is used as a research compound for exploring its potential pharmacological properties due to its structural resemblance to trozamicol, a known cognitive enhancer and memory booster. (3-iodobenzyl)trozamicol's unique properties, stemming from the addition of an iodine atom to the benzene ring, make it a promising candidate for the development of new therapeutic agents in the field of cognitive enhancement and neuropharmacology.
Used in Drug Development:
In the drug development industry, (3-iodobenzyl)trozamicol is utilized as a starting point for the creation of novel therapeutic agents. Its synthesis and characterization can provide valuable insights into the development of new drugs targeting cognitive enhancement and neuropharmacological applications. (3-iodobenzyl)trozamicol's unique structural features may offer advantages over existing drugs, potentially leading to more effective treatments for various cognitive and neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 148519-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,5,1 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 148519-95:
(8*1)+(7*4)+(6*8)+(5*5)+(4*1)+(3*9)+(2*9)+(1*5)=163
163 % 10 = 3
So 148519-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H29IN2O/c24-21-8-4-5-18(15-21)16-25-12-11-23(27)22(17-25)26-13-9-20(10-14-26)19-6-2-1-3-7-19/h1-8,15,20,22-23,27H,9-14,16-17H2/t22-,23-/m0/s1

148519-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-1-[(3-iodophenyl)methyl]-3-(4-phenylpiperidin-1-yl)piperidin-4-ol

1.2 Other means of identification

Product number -
Other names Mibt-3

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:148519-95-3 SDS

148519-95-3Upstream product

148519-95-3Downstream Products

148519-95-3Relevant academic research and scientific papers

Nonsymmetrical bipiperidyls as inhibitors of vesicular acetylcholine storage

Efange,Khare,Parsons,Bau,Metzenthin

, p. 985 - 989 (1993)

Introduction of a nitrogen atom into the cyclohexane ring of 2-(4- phenylpiperidinyl)cyclohexanol (vesamicol, AH5183) yielded two positional isomers, 5-azavesamicol (5, prezamicol) and 4-azavesamicol (6, trozamicol). As inhibitors of vesicular acetylcholi

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