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106664-96-4

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106664-96-4 Usage

Description

Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester, also known as Dipyrromethene 2.1 (1,9-nonanedicarboxylic acid) or DCMC9, is a chemical compound that serves as a key building block in the synthesis of dyes and pigments. It is a derivative of dipyrromethene, which is renowned for its fluorescent properties. This bright yellow solid exhibits a high melting point and is widely utilized in the production of fluorescent dyes for various imaging and labeling applications.

Uses

Used in Fluorescent Dye Production:
Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester is used as a key intermediate in the synthesis of fluorescent dyes, particularly for imaging and labeling applications. Its fluorescent properties make it a valuable component in creating dyes that can be used to visualize and track specific molecules or structures within various scientific and medical fields.
Used in Organic Chemistry:
In the field of organic chemistry, Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester is used as a building block for the synthesis of various functional materials. Its unique structure and properties allow it to be incorporated into a wide range of compounds, contributing to the development of new materials with diverse applications.
Used in Optical Materials Development:
Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester is used as a component in the development of optical materials due to its fluorescent properties. These materials can be utilized in various applications, such as in the creation of advanced sensors, electronic devices, and other technologies that rely on light emission or detection.
Used in Sensor Technology:
The fluorescent properties of Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester make it a valuable component in the development of sensor technology. It can be used to create sensors that are capable of detecting specific substances or changes in their environment, with potential applications in environmental monitoring, medical diagnostics, and other fields.
Used in Electronic Devices:
Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester's fluorescent properties also contribute to its use in the development of electronic devices. It can be incorporated into devices such as organic light-emitting diodes (OLEDs) and other optoelectronic components, enhancing their performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 106664-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106664-96:
(8*1)+(7*0)+(6*6)+(5*6)+(4*6)+(3*4)+(2*9)+(1*6)=134
134 % 10 = 4
So 106664-96-4 is a valid CAS Registry Number.

106664-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2,5-dioxopyrrolidin-1-yl) nonanedioate

1.2 Other means of identification

Product number -
Other names Nonanedioic acid 1,9-bis(2,5-dioxo-1-pyrrolidinyl) ester

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:106664-96-4 SDS

106664-96-4Relevant articles and documents

The use of small molecule probes to study spatially separated stimulus-induced signaling pathways

Kravchenko, Vladimir V.,Gloeckner, Christian,Stowe, G. Neil,Kang, Young J.,Tobias, Peter S.,Mathison, John C.,Ulevitch, Richard J.,Kaufmann, Gunnar F.,Janda, Kim D.

supporting information; experimental part, p. 2043 - 2045 (2012/04/23)

Simultaneous activation of signaling pathways requires dynamic assembly of higher-order protein complexes at the cytoplasmic domains of membrane-associated receptors in a stimulus-specific manner. Here, using the paradigm of cellular activation through cy

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