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(1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide is a quaternary ammonium salt with a molecular formula of C9H18IN. It features a bicyclic structure, comprising a seven-membered ring with a nitrogen atom and a six-membered ring. The iodide ion confers a net positive charge to the compound, resulting in a stable salt. This chiral compound is characterized by its specific stereochemistry, with the 1S, 2R, and 4R configurations.

4492-26-6

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4492-26-6 Usage

Uses

Used in Organic Synthesis:
(1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide is utilized as a chiral resolving agent in organic synthesis, facilitating the production of enantiomerically pure compounds. Its unique stereochemistry allows for selective reactions, which is crucial for obtaining specific enantiomers in various chemical processes.
Used in Asymmetric Synthesis:
In asymmetric synthesis, (1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide serves as a reagent, enabling the creation of chiral centers in target molecules with high enantioselectivity. This is particularly important in the synthesis of biologically active compounds, where the stereochemistry can significantly influence the compound's activity and efficacy.
Used in Pharmaceutical Industry:
(1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide is employed in the pharmaceutical industry for the production of enantiopure compounds. Many drugs exhibit different pharmacological activities based on their stereochemistry, and (1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide aids in ensuring that the desired enantiomer is synthesized, contributing to the development of more effective and safer medications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide is used for the synthesis of enantiomerically pure pesticides and agrochemicals. The ability to produce specific enantiomers can lead to more targeted and environmentally friendly products, reducing the impact on non-pest species.
Used in Medicinal Chemistry:
(1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide is also applied in medicinal chemistry, where it can be used to study the interactions between chiral compounds and biological targets. Understanding these interactions can lead to the design of more effective drugs with fewer side effects.
Used in Biochemical Research:
In biochemical research, (1S,2R,4R)-2-ethyl-2-methyl-2-azoniabicyclo[2.2.1]heptane iodide can be used as a tool to investigate enzyme selectivity, binding preferences, and the role of stereochemistry in biological processes. Such research can provide insights into the development of new drugs and a better understanding of biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 4492-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4492-26:
(6*4)+(5*4)+(4*9)+(3*2)+(2*2)+(1*6)=96
96 % 10 = 6
So 4492-26-6 is a valid CAS Registry Number.

4492-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-3-methyl-3-azoniabicyclo[2.2.1]heptane,iodide

1.2 Other means of identification

Product number -
Other names 2-Azoniabicyclo[2.2.1]heptane,iodide

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:4492-26-6 SDS

4492-26-6Upstream product

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