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Home > Encyclopedia > 2,3-DIBROMOPENTANE

2,3-DIBROMOPENTANE

2,3-DIBROMOPENTANE structure

2,3-DIBROMOPENTANE 

structure
  • CAS No:

    5780-13-2

  • Formula:

    C5H10Br2

  • Chemical Name:

    2,3-DIBROMOPENTANE

  • Synonyms:

    2,3-DIBROMOPENTANE;MESO-2,3-DIBROMOBUTANE;erythro-2,3-Dibromobutane;butane,2,3-dibromo-,meso-;(R*,S*)-2,3-dibromobutane;(2R,3S)-2,3-Dibromobutane;meso-2,3-Dibromobutane 98%;butane,2,3-dibromo-,(R*,S*)-;Butane, 2,3-dibromo-, erythro

  • Categories:

    Organic Chemistry  >  Hydrocarbons and Derivatives

2,3-DIBROMOPENTANE Basic Attributes

229.94

213.89900

226-476-1

Characteristics

0

2.55320

1.774g/cm3

-34.5°C

91 °C(lit.)

>230 °F

n20/D 1.508(lit.)

Safety Information

III

6.1(b)

2810

3

36/37/38-36

26-36-37/39

Xi

P305 + P351 + P338

H319

|Warning|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P264, P280, P305+P351+P338, and P337+P313|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory.

2,3-DIBROMOPENTANE Use and Manufacturing

1,1'-Diethyl-2,2'-dicarbocyanine iodide, a widely influential organic dye, plays a crucial role in several scientific and technological fields due to its unique chemical structure and optical properties. This compound, with its excellent dyeing ability and photosensitive properties, opens up new ways for scientific research and industrial applications. In biomedical research, 1,1' -diethyl-2,2'-dicarbocyanine iodide is favored for its efficient cell penetration and low toxicity. As a cell stain, it is able to accurately label and visualize cell membranes and nuclei, providing a powerful tool for cell biology research. In molecular diagnostics, it is used as a fluorescent probe that can specifically identify and label cancer cells, enabling early diagnosis and disease monitoring. In addition, its application in photodynamic therapy is also becoming increasingly prominent, through the photoinduced chemical reaction, can effectively kill tumor cells, providing a new strategy for cancer treatment. In the field of optoelectronics, 1,1' -diethyl-2,2'-dicarbocyanine iodide is equally widely used. In dye-sensitized solar cells, it can effectively absorb sunlight and promote the generation of electrons, thereby improving the photoelectric conversion efficiency of the battery, providing new possibilities for the development of renewable energy. At the same time, as a photosensitive material, it also has a wide range of applications in photodetectors and optical recording media, and can achieve efficient capture and storage of optical signals. In laser technology, because of its broad absorption spectrum and good laser characteristics, the compound is often used as a laser dye for the manufacture of solid-state lasers capable of producing various wavelengths, meeting the needs of scientific research and industry for accurate spectral control. In addition, 1,1'-Diethyl-2,2'-dicarbocyanine iodide also shows great potential in the fields of chemical sensing, photochromic materials, and fluorescent probes. For example, as a chemical sensor, it can respond sensitively to specific chemicals, providing new solutions for environmental monitoring and industrial process control. Its photochromic properties make it have potential application value in intelligent Windows, information storage and other fields. With the continuous progress of science and technology and the in-depth exploration of new functional materials, the application field of 1,1'-Diethyl-2,2'-dicarbocyanine iodide will be further expanded, and its importance in optoelectronics, biomedicine, energy science and other interdisciplinary disciplines will be more prominent. The future development prospect of this multifunctional organic dye is expected, and it will make greater contributions to the scientific and technological progress and sustainable development of human society.

Computed Properties

Molecular Weight:215.91
XLogP3:2.6
Rotatable Bond Count:1
Exact Mass:215.89723
Monoisotopic Mass:213.89928
Heavy Atom Count:6
Complexity:30.5
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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