4044-58-0 Usage
Description
1-Bromo-8-iodonaphthalene is a chemical compound with the molecular formula C10H6BrI. It is a naphthalene derivative that contains both bromine and iodine atoms, known for its unique chemical properties. 1-Bromo-8-iodonaphthalene is recognized for its potential applications in various scientific fields, including medicinal chemistry and materials science, due to its distinctive characteristics.
Uses
Used in Organic Synthesis:
1-Bromo-8-iodonaphthalene is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its presence in the molecular structure allows for a variety of chemical reactions to take place, facilitating the creation of new compounds with specific properties.
Used in Chemical Reactions:
As a reagent, 1-Bromo-8-iodonaphthalene is utilized in various chemical reactions to modify or create new chemical entities. Its bromine and iodine atoms make it a versatile component in the synthesis process, enabling the development of a wide range of products.
Used in Pharmaceutical Synthesis:
1-Bromo-8-iodonaphthalene is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their efficacy or modifying their properties to treat specific medical conditions.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-Bromo-8-iodonaphthalene is employed in the development of new pesticides or herbicides. Its chemical properties can be leveraged to create compounds that are effective in controlling pests or unwanted plant growth, contributing to agricultural productivity.
Used in Medicinal Chemistry Research:
1-Bromo-8-iodonaphthalene is used as a research compound in medicinal chemistry. Its unique properties make it a candidate for studying the interactions with biological targets, potentially leading to the discovery of new therapeutic agents.
Used in Materials Science:
In the field of materials science, 1-Bromo-8-iodonaphthalene is used to explore its potential in creating new materials with specific characteristics. Its chemical structure may contribute to the development of materials with unique electronic, optical, or mechanical properties.
It is important to handle 1-Bromo-8-iodonaphthalene with care due to its potential hazards if not properly managed, emphasizing the need for safety precautions in its application and manipulation.
Check Digit Verification of cas no
The CAS Registry Mumber 4044-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4044-58:
(6*4)+(5*0)+(4*4)+(3*4)+(2*5)+(1*8)=70
70 % 10 = 0
So 4044-58-0 is a valid CAS Registry Number.
4044-58-0Relevant articles and documents
Photodissociation of B-N Lewis adducts: A partially fused trinaphthylborane with dual fluorescence
Matsuo, Kyohei,Saito, Shohei,Yamaguchi, Shigehiro
, p. 12580 - 12583 (2014)
The synthesis of a planarized trinaphthylborane with partially fused structure is presented. This compound shows not only high chemical and thermal stability but also sufficient Lewis acidity to form Lewis adducts with pyridine derivatives in solution. The B-N Lewis adducts exhibit unprecedented photodissociation behavior in the excited state, reminiscent of the photogeneration of carbenium ions from triarylmethane leuco dyes. Consequently, these B-N Lewis adducts exhibit dual fluorescence emission arising from the initial tetracoordinate B-N adducts and the photodissociated tricoordinate boranes.
Divergent intramolecular reactions between phosphines and alkynes
Song, Yanying,Wang, Lili,Duan, Zheng,Mathey, Fran?ois
supporting information, p. 329 - 332 (2019/06/18)
A divergent intramolecular reaction of phosphine tethered alkyne in protic solvent was developed. This provided a novel and simple access to a large variety of (Z)-alkenylphosphine oxides and phospholane oxides. Our preliminary studies suggested that these divergent reactions are closely related to the reaction condition and molecular structure. A possible mechanism of C-P bond cleavage of a pentacoordinated hydroxyphosphorane intermediate was proposed.
Paving the Way to Novel Phosphorus-Based Architectures: A Noncatalyzed Protocol to Access Six-Membered Heterocycles
Romero-Nieto, Carlos,Lpez-Andarias, Alicia,Egler-Lucas, Carolina,Gebert, Florian,Neus, Jens-Peter,Pilgram, Oliver
supporting information, p. 15872 - 15875 (2016/01/28)
Phosphorus-based heterocycles provide access to materials with properties that are inaccessible from all-carbon architectures. The unique hybridization of phosphorus gives rise to electron-accepting capacities, a large variety of coordination reactions, a
