2914-72-9 Usage
Description
(3-NITRO-PHENYL)-(4-NITRO-PHENYL)-ETHER is a nitro-substituted phenyl ether, characterized by a molecule with a nitro group attached to the 3-position of one phenyl ring and another nitro group attached to the 4-position of a second phenyl ring. This yellow crystalline solid has the molecular formula C12H8N2O5 and is utilized in organic chemistry and pharmaceutical research as a building block for synthesizing various compounds. Due to the presence of nitro groups, it is also a potential source of nitroaromatic pollutants, necessitating careful handling and disposal to mitigate ecological and health impacts.
Uses
Used in Organic Chemistry:
(3-NITRO-PHENYL)-(4-NITRO-PHENYL)-ETHER is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Research:
In pharmaceutical research, (3-NITRO-PHENYL)-(4-NITRO-PHENYL)-ETHER serves as a key intermediate in the synthesis of pharmaceuticals, potentially leading to the discovery of new drugs and therapeutic agents.
Used in Environmental Management:
Given its potential to contribute to nitroaromatic pollution, (3-NITRO-PHENYL)-(4-NITRO-PHENYL)-ETHER is also relevant in the field of environmental management, where its proper handling and disposal are crucial to prevent ecological and health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 2914-72-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2914-72:
(6*2)+(5*9)+(4*1)+(3*4)+(2*7)+(1*2)=89
89 % 10 = 9
So 2914-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N2O5/c15-13(16)9-4-6-11(7-5-9)19-12-3-1-2-10(8-12)14(17)18/h1-8H
2914-72-9Relevant articles and documents
CsF/clinoptilolite: An efficient solid base in SNAr and copper-catalyzed Ullmann reactions
Keipour, Hoda,Hosseini, Abolfazl,Afsari, Amir,Oladee, Razieh,Khalilzadeh, Mohammad A.,Ollevier, Thierry
, p. 95 - 104 (2016/01/16)
CsF/clinoptilolite was found to be an efficient solid base catalyst for both SNAr and Ullmann ether reactions. A general and efficient one-step procedure was developed for the synthesis of biaryl ethers via direct coupling of electron-deficient aryl halides to phenols using CsF/clinoptilolite. The protocol was also applied to electron-rich aryl halides by addition of a catalytic amount of copper oxide nanoparticles. Both SNAr and Ullmann reactions were rapid and provided good to excellent yields.