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2-Thiophenemethanol, 4,4'-(1-cyclopentene-1,2-diyl)bis[5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

876928-77-7

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876928-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876928-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,9,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 876928-77:
(8*8)+(7*7)+(6*6)+(5*9)+(4*2)+(3*8)+(2*7)+(1*7)=247
247 % 10 = 7
So 876928-77-7 is a valid CAS Registry Number.

876928-77-7Upstream product

876928-77-7Downstream Products

876928-77-7Relevant academic research and scientific papers

Monomeric and aggregation emissions of tetraphenylethene in a photo-switchable polymer controlled by cyclization of diarylethene and solvent conditions

Singh, Ravinder,Wu, Hsin-Yen,Kumar Dwivedi, Atul,Singh, Ashutosh,Lin, Chien-Min,Raghunath, Putikam,Lin, Ming-Chang,Wu, Tung-Kung,Wei, Kung-Hwa,Lin, Hong-Cheu

, p. 9952 - 9962 (2017)

A novel photo-switchable polymer P-PHT containing diarylethene (DAE) and tetraphenylethene (TPE) moieties and a triazole linker in the repeating unit was synthesized to study the aggregation-induced emission (AIE) behaviour of TPE with both the open and closed forms of DAE in P-PHT with high water contents. The photo-switching phenomena of DAE (from open to closed forms under UV-irradiation) in P-PHT were prominent in organic solvent (THF), high water contents (at 90% H2O) and acidic conditions. Upon UV-irradiation of P-PHT at 90% water content, the AIE of TPE was completely quenched via an energy transfer event from TPE to cyclized DAE. Interestingly, the rare monomeric emission of TPE was first discovered by the photo-cyclization of DAE in P-PHT compared with the AIE behaviour of TPE with the open form of DAE in P-PHT with AIE favourable conditions of high water content (90% H2O) and acidic conditions.

Diarylethene compound, preparation and applications thereof

-

, (2020/01/25)

The invention relates to a diarylethene compound, preparation and applications thereof, and specificallydiscloses a compound represented by a formula (A), wherein various groups are defined in the specification. According to the invention, the compound is an excellent photochromic compound, and can be subjected to a photoisomerization reaction under the irradiation of light with specific wavelength to generate a ring-closing compound; and the compound and the photoisomerized ring-closing derivative thereof have high activity on agricultural and forestry pests such as aphids, aedes albopictus larvae of NematoceraCulicidae, and the like, and the activity of the ring-closing compound after illumination is higher than the activity of the ring-opening compound before illumination.

Diarylethene type photochromic insecticidal compound and preparation method and purpose thereof

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, (2017/06/20)

The invention relates to a diarylethene type photochromic insecticidal compound and a preparation method and a purpose thereof. Specifically, the invention discloses a compound as shown in formula (A) or an optical isomer or a cis-trans-isomer thereof, or an agricultural pharmaceutically acceptable salt, and the definitions of substituent groups are as stated in the description. The invention also discloses the preparation method and the purpose of the compound. The formula (A) is shown in the description.

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