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4727-50-8

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4727-50-8 Usage

Description

1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE, also known as a cationic C3-cyanine type compound, is characterized by its 1-ethylquinolin-4-yl groups at both ends. It is a dark green fine crystalline powder, known for its solubility and unique properties that make it suitable for various applications.

Uses

Used in Laser Operations:
1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE is used as a chemical shutter in laser operations due to its ability to control the flow of light, making it a valuable component in the field of optics and photonics.
Used as a Laser Dye:
In the field of laser technology, 1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE serves as a laser dye, enhancing the performance and efficiency of laser systems by providing the necessary color and energy transfer properties.
Used in Chemical Research:
As an organic dye with specific chemical properties, 1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE is also utilized in chemical research for various purposes, including the study of molecular interactions and the development of new materials and technologies.
Used in Analytical Chemistry:
1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE's solubility and unique characteristics make it suitable for use in analytical chemistry, where it can be employed as a reagent or indicator in various chemical analyses and assays.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, due to its cationic nature and potential interactions with biological systems, 1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE may also find applications in the pharmaceutical industry, possibly as a component in drug delivery systems or as a marker in biological imaging techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 4727-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4727-50:
(6*4)+(5*7)+(4*2)+(3*7)+(2*5)+(1*0)=98
98 % 10 = 8
So 4727-50-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H26N2/c1-3-26-18-16-20(22-12-5-7-14-24(22)26)10-9-11-21-17-19-27(4-2)25-15-8-6-13-23(21)25/h5-19,24H,3-4H2,1-2H3/b10-9+,21-11+

4727-50-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H55456)  1,1'-Diethyl-4,4'-carbocyanine iodide, 96%   

  • 4727-50-8

  • 250mg

  • 259.0CNY

  • Detail
  • Alfa Aesar

  • (H55456)  1,1'-Diethyl-4,4'-carbocyanine iodide, 96%   

  • 4727-50-8

  • 1g

  • 659.0CNY

  • Detail
  • Alfa Aesar

  • (H55456)  1,1'-Diethyl-4,4'-carbocyanine iodide, 96%   

  • 4727-50-8

  • 5g

  • 2968.0CNY

  • Detail
  • Aldrich

  • (D91535)  1,1′-Diethyl-4,4′-carbocyanineiodide  96%

  • 4727-50-8

  • D91535-250MG

  • 462.15CNY

  • Detail

4727-50-8Relevant articles and documents

The third-order nonlinear optical properties of charge flowable trimethine cyanine with quinolone groups

Miao, Jia-Tao,Wu, Xing-Zhi,Sun, Ru,Song, Ying-Lin,Ge, Jian-Feng

, p. 41 - 46 (2014/03/21)

Organic molecules with charge flow abilities gain much attention in third-order nonlinear optical materials. To evaluate the hypothesis of terminal donor and/or acceptor groups participating organic resonance structures for third-order nonlinear optical materials, conjugated double bonds structures with terminal amino groups are selected in this paper. The trimethine cyanine dye with quinolone skeleton (3a) was synthesized, it shows strong reverse saturable absorption and nonlinear refraction in dimethyl formamide solution at 532 nm. Then, its derivative compound (3b) with long alkyl chains was synthesized in order to improve the film forming performance, the spinning coating thin film exhibits strong reverse saturable absorption with the third-order nonlinear susceptibilities χI(3)=3.42×10-8esu and χ( 3)=3.23×10-9esu under nanosecond and picosecond laser beams respectively. The results validate that the organic compounds with terminal donor and/or acceptor groups participating resonance structures have potential value for the design of the third-order nonlinear optical materials.

CONDENSATION OF VILSMEIER COMPLEXES WITH HETEROCYCLIC COMPOUNDS. SYNTHESIS OF CARBOCYANINES

Makin, S. M.,Pomogaev, A. I.

, p. 1916 - 1918 (2007/10/02)

Carbocyanine dyes are formed in the reaction of the quaternary salts of heterocyclic bases containing an active methyl group with the complexes of carboxamides and phosphorus oxychloride.A series of carbocyanines were synthesized, including those containing various substituents at the meso position of the trimethine chain.

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