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2-{2-[acetyl(phenyl)amino]ethenyl}-3-methyl-1,3-benzothiazol-3-ium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62196-30-9

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62196-30-9 Usage

Structure

Benzothiazolium core with an acetylphenylamino group attached

Quaternary Ammonium Salt

Nitrogen atom in the benzothiazolium ring carries a positive charge

Functional Groups

Acetyl group: Derived from acetic acid
Phenylamino group: Derived from a phenylamine

Properties

Positive charge on nitrogen
Aromatic ring system
Ethenyl and methyl substituents

Potential Uses

Chemical processes
Pharmaceuticals
Other applications requiring unique chemical structures and interactions

Check Digit Verification of cas no

The CAS Registry Mumber 62196-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62196-30:
(7*6)+(6*2)+(5*1)+(4*9)+(3*6)+(2*3)+(1*0)=119
119 % 10 = 9
So 62196-30-9 is a valid CAS Registry Number.

62196-30-9Relevant academic research and scientific papers

A comparative study of symmetrical and unsymmetrical trimethine cyanine dyes bearing benzoxazolyl and benzothiazolyl groups

Shi, Quan-Quan,Sun, Ru,Ge, Jian-Feng,Xu, Qing-Feng,Li, Na-Jun,Lu, Jian-Mei

experimental part, p. 1506 - 1511 (2012/03/11)

Six symmetrical and unsymmetrical trimethine cyanine dyes bearing benzothiazolyl and benzoxazolyl groups were synthesized. Their linear optical properties were studied. It was found that the variation of hetero atoms play an important role in the spectral properties of the dyes. Sequential replacement of the oxygen atom by the sulfur atom resulted in a change in shade from yellow to purple. In order to understand the relationship between the molecular structures and the spectral properties of these dyes, theoretical calculations were made using the Gaussian programme. Key parameters related to absorption and emission spectra were reported and discussed.

Hybridization-sensitive fluorescence control in the near-infrared wavelength range

Ikeda, Shuji,Yanagisawa, Hiroyuki,Nakamura, Akiko,Wang, Dan Ohtan,Yuki, Mizue,Okamoto, Akimitsu

experimental part, p. 4199 - 4204 (2011/06/25)

A series of near-infrared fluorescent probes were designed based on the concept of emission control caused by interdye excitonic interaction. The fluorescent probes showed very weak emission in the unhybridized state, whereas they emitted near-infrared fl

Cyanine dye conjugates as probes for live cell imaging

Carreon, Jay R.,Stewart, Kelly M.,Mahon Jr., Kerry P.,Shin, Stephanie,Kelley, Shana O.

, p. 5182 - 5185 (2008/03/13)

A series of fluorescent compounds suitable for live cell imaging is described. Functionalized forms of four different asymmetric cyanine dyes are reported that are amenable to peptide conjugation. The photophysical properties of the modified dyes and conj

PHOTOTOXIC COMPOUNDS

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Page/Page column 37, (2010/02/15)

The invention discloses various phototoxic compounds which include a photosensitizer conjugated to a peptide or peptoid. Additionally, the invention discloses a method of making and using the various phototoxic compound. Furthermore, the invention disclos

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