34596-36-6 Usage
Description
1,4-Bis(2-propynyloxy)benzene, also known as 1,4-bis(prop-2-ynoxy)benzene, is an organic compound characterized by its unique structure that features two propynyloxy groups attached to a benzene ring at the 1,4 positions. 1,4-Bis(2-propynyloxy)benzene is known for its reactivity and potential applications in various fields due to its versatile chemical properties.
Uses
1. Used in the Preparation of Nanoparticles:
1,4-Bis(2-propynyloxy)benzene is used as a reactant for the preparation of nano-CeO2 particles. These nanoparticles are capped with galactose functionalized pillar[5]arene, which enhances their properties and potential applications in various industries.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Bis(2-propynyloxy)benzene can be utilized as a key intermediate in the synthesis of various drugs and drug candidates. Its unique structure allows for the development of new molecules with potential therapeutic properties.
3. Used in Chemical Synthesis:
1,4-Bis(2-propynyloxy)benzene is used as a building block in the synthesis of complex organic molecules, including those with potential applications in materials science, electronics, and other advanced technologies.
4. Used in Research and Development:
Due to its unique structure and reactivity, 1,4-Bis(2-propynyloxy)benzene is a valuable compound for research and development purposes. It can be used to explore new reaction pathways, develop novel synthetic methods, and create new materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 34596-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,9 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34596-36:
(7*3)+(6*4)+(5*5)+(4*9)+(3*6)+(2*3)+(1*6)=136
136 % 10 = 6
So 34596-36-6 is a valid CAS Registry Number.
34596-36-6Relevant articles and documents
Synthesis, structure and tunable shape memory properties of polytriazoles: Dual-trigger temperature and repeatable shape recovery
Ragin Ramdas,Santhosh Kumar,Reghunadhan Nair
, p. 11596 - 11606 (2015)
Thermally induced shape memory polymers (SMPs) are capable of storage, release of energy and shape recovery on the macro-scale. In this work, cross-linked SMPs were synthesized from the monomers tris(4-(1-azido 3-oxy propan-2-ol)phenyl) methane (A3/
Synthesis and characterization of novel phenoxy-substituted enediyne-triazole conjugates using click chemistry
Joshi, Mukesh C.
, p. 195 - 202 (2021/03/19)
Novel group of phenoxy-substituted enediyne-triazole conjugates were synthesized by Huisgen [3+2] cycloaddition reaction (Click chemistry) in aqueous media. It was observed that ene-diynes were stable in aqueous medium and open-air conditions.
Synergetic effects in the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid mediated by β-cyclodextrin-pillar[5]arene-hybridized hosts
Cheng, Guo,Gong, Qiyong,Ji, Jiecheng,Luo, Kui,Rao, Ming,Wei, Xueqin,Wu, Wanhua,Yang, Cheng,Zhou, Dayang
supporting information, p. 6197 - 6200 (2020/06/22)
Tri-cavity hosts consisting of one pillar[5]arene (P5) sandwiched by two β-cyclodextrins (CDs) were synthesized, and their diastereoseparation was successfully accomplished. Photocyclodimerization of 2-anthracenecarboxylate with these hybrid hosts demonst