2-Bromoselenophene

  • CasNo:1449-68-9
  • purity:99%
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What is the 2-Bromoselenophene ?

2-Bromoselenophene is , while it's Molecular Formula is C4H3 Br Se. Used in Organic Chemistry:
2-Bromoselenophene is used as a key intermediate in the synthesis of complex organic molecules, particularly for the creation of biologically active compounds. Its electrophilic nature, due to the bromine atom, facilitates cross-coupling reactions, making it a valuable component in organic synthesis.
Used in Pharmaceutical Industry:
2-Bromoselenophene is used as a building block for the development of pharmaceutical compounds. Its reactivity in cross-coupling reactions allows for the formation of diverse molecular structures with potential therapeutic applications.
Used in Material Science:
2-Bromoselenophene is used as a component in the synthesis of advanced materials, such as polymers and nanomaterials, that exhibit unique properties. Its chemical stability and reactivity contribute to the development of materials with potential applications in various industries.
Safety Precautions:
When working with 2-Bromoselenophene, appropriate caution should be taken, as with all chemicals. This includes the use of personal protective equipment and working in a well-ventilated space to minimize potential health risks. Due to its limited information regarding toxicity and handling precautions, it is essential to follow standard safety protocols and consult relevant safety data sheets for additional guidance.

What is the CAS number for 2-Bromoselenophene ?

The CAS number of 2-Bromoselenophene is 1449-68-9.

More information of 2-Bromoselenophene 1449-68-9 are:

Synonyms

2-Bromoselenophene

CAS?Number

1449-68-9

Molecular Formula

C4H3 Br Se

Molecular Weight

209.932

Boiling Point

187.5°C at 760 mmHg

Flash Point

67.2°C

HS CODE

2903399090

PSA

0.00000

LogP

1.50610

What is 2-Bromoselenophene (1449-68-9) used for?

2-Bromoselenophene is an organoselenium compound that belongs to the class of organobromides. It is predominantly utilized in the field of organic chemistry and typically appears as a crystalline solid. Known for its impressive chemical stability, it is relatively unreactive but plays a crucial role in various chemical reactions, particularly in processes that involve cross-coupling. Its bromine atom makes it an excellent electrophile, which is highly valuable in the creation of various biologically active compounds.

InChI:InChI=1/C4H3BrSe/c5-4-2-1-3-6-4/h1-3H

Articles related to 2-Bromoselenophene:

Article

Source

The Origin of Chalcogen-Bonding Interactions

Pascoe, Dominic J.,Ling, Kenneth B.,Cockroft, Scott L.

, p. 15160 - 15167 (2017)

Asymmetric Heteroleptic Ir(III) Phosphorescent Complexes with Aromatic Selenide and Selenophene Groups: Synthesis and Photophysical, Electrochemical, and Electrophosphorescent Behaviors

Feng, Zhao,Wang, Dezhi,Yang, Xiaolong,Jin, Deyuan,Zhong, Daokun,Liu, Boao,Zhou, Guijiang,Ma, Miaofeng,Wu, Zhaoxin

, p. 11027 - 11043 (2018/09/14)

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