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1-[(E)-3-{4-[2-(2,5-Dimethyl-thiophen-3-yl)-3,3,4,4,5,5-hexafluoro-cyclopent-1-enyl]-5-methyl-thiophen-2-yl}-3-phenyl-prop-2-en-(Z)-ylidene]-1H-naphthalen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868134-73-0

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868134-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868134-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,1,3 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 868134-73:
(8*8)+(7*6)+(6*8)+(5*1)+(4*3)+(3*4)+(2*7)+(1*3)=200
200 % 10 = 0
So 868134-73-0 is a valid CAS Registry Number.

868134-73-0Relevant academic research and scientific papers

Multiple addressing in a hybrid biphotochromic system

Frigoli, Michel,Mehl, Georg H.

, p. 5048 - 5052 (2005)

Affairs of state: Investigation of the photochromic properties of a combined naphthopyran and diarylethene biphotochromic system (1) has revealed that four different states with entirely different absorption behaviors are formed. Opening of the naphthopyr

Controlled conversion of isomers in a hybrid biphotochromic system

Delbaere, Stephanie,Vermeersch, Gaston,Frigoli, Michel,Mehl, Georg H.

, p. 4931 - 4934 (2006)

(Chemical Equation Presented) The photochromic performance of a hybrid system connecting naphthopyran and dithienylethene was investigated, and the photochemistry of eight different isomers was explored by choosing an appropriate wavelength of light.

Mechanistic understanding of the photochromism of a hybrid dithienylethene-naphthopyran system by NMR spectroscopy

Delbaere,Micheau,Frigoli,Mehl,Vermeersch

, p. 929 - 935 (2007)

Detailed 1H NMR kinetic investigations of the photochemical and thermal behaviour of a recently described poly-photochromic molecule including both dithienylethene and naphthopyran groups are reported. The combination of two photochromic moieties allows the selective controlled extension of the conjugated pi-electron system and the modulation of the absorption behaviour between ~380 to ~750nm. It is shown that the two photochromic entities are coupled and do not behave independently. Copyright

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