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31661-59-3

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31661-59-3 Usage

General Description

1,4-BIS(3-aminophenyl)butadiyne is a chemical compound that belongs to the group of bis(arylethynyl)benzene derivatives. It is composed of a butadiyne core with two 3-aminophenyl groups attached to the terminal positions. This chemical is commonly used as a crosslinking agent in the production of polymers, particularly in the field of organic electronics and optoelectronics. It has also been studied for its potential applications in nonlinear optical materials and molecular electronics due to its high thermal stability and conjugated structure. Additionally, 1,4-BIS(3-aminophenyl)butadiyne has shown promise as a potential building block for the construction of advanced materials with tailored properties for various technological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31661-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,6 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31661-59:
(7*3)+(6*1)+(5*6)+(4*6)+(3*1)+(2*5)+(1*9)=103
103 % 10 = 3
So 31661-59-3 is a valid CAS Registry Number.

31661-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(3-aminophenyl)buta-1,3-diynyl]aniline

1.2 Other means of identification

Product number -
Other names 1,4-bis(m-aminophenyl)buta-1,3-diyne

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:31661-59-3 SDS

31661-59-3Relevant articles and documents

High-efficiency catalyst for copper nanoparticles attached to porous nitrogen-doped carbon materials: Applied to the coupling reaction of alkyne groups under mild conditions

Ma, Lei,Jiang, Pengbo,Wang, Kaizhi,Huang, Xiaokang,Yang, Ming,Gong, Li,Li, Rong

, (2021)

Supported catalysts have attracted extensive attention due to their excellent catalytic performance and reliability in heterogeneous catalysis. In this work, we report a general synthesis strategy that achieves the self-coupling reaction of acetylene deri

Creating Dynamic Nanospaces in Solution by Cationic Cages as Multirole Catalytic Platform for Unconventional C(sp)?H Activation Beyond Enzyme Mimics

Li, Kang,Wu, Kai,Lu, Yu-Lin,Guo, Jing,Hu, Peng,Su, Cheng-Yong

supporting information, (2021/12/14)

Herein we demonstrate that, based on the creation of dynamic nanospaces in solution by highly charged positive coordination cage of [Pd6(RuL3)8]28+, multirole and multi-way cage-confined catalysis is accomplisha

Leaf-like CuO nanosheets on rGO as an efficient heterogeneous catalyst for Csp-Csp homocoupling of terminal alkynes

Gao, Lingfeng,Wang, Bin,Zheng, Gengxiu

, (2020/12/21)

In this work, the economic and well-defined leaf-like CuO nanosheets on rGO (CuO nanosheets/rGO) was synthesized by a convenient hydrothermal method. The morphology and chemical composition of CuO nanosheets/rGO were confirmed by XRD, SEM-EDS, TEM, HR-TEM, and XPS techniques. The CuO nanosheets/rGO was successfully applied as a high-performance heterogeneous catalyst in the homocoupling of 12 terminal alkynes, and the isolated yield of each product was more than 80%, except for propargyl alcohol. This catalyst could be reused five times with little activity loss. Thus, it is beneficial for green and sustainable development of organic synthetic chemistry.

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