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p-hydroxyphenyl 9-bromononyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132568-33-3

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132568-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132568-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,6 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132568-33:
(8*1)+(7*3)+(6*2)+(5*5)+(4*6)+(3*8)+(2*3)+(1*3)=123
123 % 10 = 3
So 132568-33-3 is a valid CAS Registry Number.

132568-33-3Relevant academic research and scientific papers

Near infrared light-driven liquid crystal phase transition enabled by hydrophobic mesogen grafted plasmonic gold nanorods

Gutierrez-Cuevas, Karla G.,Wang, Ling,Xue, Chenming,Singh, Gautam,Kumar, Satyendra,Urbas, Augustine,Li, Quan

, p. 9845 - 9848 (2015)

Light-driven phase transition in liquid crystals is a fascinating endeavour from both scientific and technological points of view. Here we demonstrate the proof-of-principle that the photothermal effect of organo-soluble plasmonic gold nanorods can introd

NIR light-directing self-organized 3D photonic superstructures loaded with anisotropic plasmonic hybrid nanorods

Wang, Ling,Gutierrez-Cuevas, Karla G.,Bisoyi, Hari Krishna,Xiang, Jie,Singh, Gautam,Zola, Rafael S.,Kumar, Satyendra,Lavrentovich, Oleg D.,Urbas, Augustine,Li, Quan

, p. 15039 - 15042 (2015)

Self-organized 3D photonic superstructures loaded with plasmonic hybrid nanorods were found to undergo structural transformation from body-centered cubic to simple cubic upon NIR-light irradiation resulting from the "photothermal effect" of gold nanorods.

Enantioselective synthesis of planar-chiral 1, n -dioxa[ n ]paracyclophanes via catalytic asymmetric ortho -Lithiation

Kanda, Kazumasa,Endo, Kohei,Shibata, Takanori

, p. 1980 - 1983 (2010)

Figure presented Highly enantioselective ortho-lithiation and dilithiation of 1,n-dioxa[n]paracyclophanes were realized with the use of sec-butyllithium and a catalytic or stoichiometric amount of sparteine. Quenching with various electrophiles, such as i

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