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663610-75-1

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663610-75-1 Usage

Description

2-(Aminomethyl)-2-methyl Doxyl is a chemical compound that features an aminomethyl group attached to a 2-methyl Doxyl moiety. This structure allows for the creation of novel amphiphilic spin probes with the paramagnetic Doxyl group located in the polar region, which is crucial for their functionality in various applications.

Uses

Used in Synthesis of Amphiphilic Spin Probes:
2-(Aminomethyl)-2-methyl Doxyl is used as a key component in the synthesis of novel amphiphilic spin probes. The presence of the paramagnetic Doxyl group in the polar region of these probes enables their use in various applications, such as studying the structure and dynamics of biomembranes and other systems.
Used in Research and Diagnostic Applications:
In the field of research and diagnostics, 2-(Aminomethyl)-2-methyl Doxyl-based spin probes are employed for their ability to provide insights into the structural and dynamic properties of biomembranes. This can be particularly useful in studying the behavior of proteins, lipids, and other biomolecules within these environments.
Used in Pharmaceutical Industry:
2-(Aminomethyl)-2-methyl Doxyl is used as a building block in the development of new pharmaceutical agents. Its unique structure allows for the design of drugs with specific targeting and delivery properties, potentially leading to more effective treatments for various diseases.
Used in Material Science:
In material science, 2-(Aminomethyl)-2-methyl Doxyl can be utilized in the development of advanced materials with unique properties. The incorporation of this compound into the structure of these materials can lead to improved performance in areas such as sensing, imaging, and drug delivery.

Check Digit Verification of cas no

The CAS Registry Mumber 663610-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,3,6,1 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 663610-75:
(8*6)+(7*6)+(6*3)+(5*6)+(4*1)+(3*0)+(2*7)+(1*5)=161
161 % 10 = 1
So 663610-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O2/c1-6(2)5-11-7(3,4-8)9(6)10/h10H,4-5,8H2,1-3H3

663610-75-1SDS

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 2-(Aminomethyl)-2-methyl Doxyl

1.2 Other means of identification

Product number -
Other names (3-hydroxy-2,4,4-trimethyl-1,3-oxazolidin-2-yl)methanamine

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:663610-75-1 SDS

663610-75-1Downstream Products

663610-75-1Relevant articles and documents

Synthesis of novel amphiphilic spin probes with the paramagnetic doxyl group in the polar region

Pajk, Stane,Pe?ar, Slavko

body text, p. 659 - 665 (2009/04/07)

The use of ESR and specially designed spin probes has led to major breakthroughs in understanding the complexity of biological membranes. Research has been focused mainly on molecular events within the?lipid bilayer, and few probes have been designed for studying events in the extracellular space near the membrane surface. We have prepared a series of amphiphilic spin probes in which an ethylene glycol type hydrophilic spacer was introduced between a hydrophobic anchor and the doxyl group, placing the latter above the membrane in the extracellular space. Furthermore, the 2pπ orbital, containing the unpaired electron of the nitroxide group, would be orientated perpendicular to the membrane surface, making it more useful for ESR investigations of structural and dynamic properties close to the membrane surface in different situations of the cell life.

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