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Benzothiazole, 2-[4-(2-phenylethenyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16178-30-6

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16178-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16178-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16178-30:
(7*1)+(6*6)+(5*1)+(4*7)+(3*8)+(2*3)+(1*0)=106
106 % 10 = 6
So 16178-30-6 is a valid CAS Registry Number.

16178-30-6Downstream Products

16178-30-6Relevant academic research and scientific papers

Facile access to libraries of diversely substituted 2-aryl-benzoxazoles/benzothiazoles from readily accessible aldimines via cyclization/cross coupling in imidazolium-ILs with Pd(OAc)2 or NiCl2 (dppp) as catalyst

Malunavar, Shruti S.,Sutar, Suraj M.,Savanur, Hemantkumar M.,Kalkhambkar, Rajesh G.,Laali, Kenneth K.

, (2019/12/24)

A two-step protocol involving Pd-catalyzed cyclization of readily accessible p-bromophenyl-aldimines to 2-bromophenyl-benzoxazole/benzothiazole in [BMIM][PF6] or [BMIM][BF4] as solvent, followed by the Suzuki, Heck, and Sonogashira cross-coupling reactions catalyzed by Pd or Ni is described that generates libraries of diversely substituted 2-aryl-/heteroaryl-benzoxazoles/benzothiazoles in respectable isolated yields under mild reaction conditions. The feasibility to perform the two-steps in sequence in one-pot starting from the aldimines is also demonstrated and the potential for recycling/reuse of the IL solvent is also shown.

Degenerate nonlinear absorption and optical power limiting properties of asymmetrically substituted stilbenoid chromophores

Lin, Tzu-Chau,He, Guang S.,Prasad, Paras N.,Tan, Loon-Seng

, p. 982 - 991 (2007/10/03)

Two-photon absorption (2PA) spectra (650-1000 nm) of a series of model chromophores were measured via a newly developed nonlinear absorption spectral technique based on a single and powerful femtosecond white-light continuum beam. The experimental results suggested that when either an electron-donor or an electron-acceptor was attached to a trans-stilbene at a para-position, an enhancement in molecular two-photon absorptivity was observed in both cases, particularly in the 650-800 nm region. However, the push-pull chromophores with both the donor and acceptor groups showed larger overall two-photon absorption cross-sections within the studied spectral region as compared to their mono-substituted analogues. The combined results of the solvent effect and the 1H-NMR studies indicated that stronger acceptors produce a more efficient intramolecular charge transfer character upon excitation, leading to increased molecular two-photon responses in this model-compound set. A fairly good 2PA based optical power limiting behavior from one of the model chromophores is also demonstrated.

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