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2-cyano-3-(4-(diphenylamino)phenyl)acrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

387844-17-9

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387844-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 387844-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,7,8,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 387844-17:
(8*3)+(7*8)+(6*7)+(5*8)+(4*4)+(3*4)+(2*1)+(1*7)=199
199 % 10 = 9
So 387844-17-9 is a valid CAS Registry Number.

387844-17-9Downstream Products

387844-17-9Relevant academic research and scientific papers

Molecular engineering of triphenylamine based aggregation enhanced emissive fluorophore: Structure-dependent mechanochromism and self-reversible fluorescence switching

Hariharan, Palamarneri Sivaraman,Prasad, Viki Kumar,Nandi, Surajit,Anoop, Anakuthil,Moon, Dohyun,Anthony, Savarimuthu Philip

, p. 146 - 155 (2017)

Triphenylamine (TPA), a propeller-shaped optoelectronic molecule, has been used to generate stimuli-responsive smart fluorescent organic materials and correlate the effect of subtle structural changes on the molecular packing and mechanochromic fluorescen

Mechanical force induced reversible fluorescence switching of two 3-aryl-2-cyano acrylamide derivatives

Song, Qingbao,Chen, Kang,Sun, Jingwei,Wang, Yongsheng,Ouyang, Mi,Zhang, Cheng

supporting information, p. 3200 - 3205 (2014/05/20)

Two structural-simple 3-aryl-2-cyano acrylamide derivatives (CDPA-E and CDPA-P) were synthesized and characterized by NMR, MS, IR, and single crystal. It was found that both of them exhibited obvious piezofluorochromic properties. The as-prepared yellow-green compounds were both converted to orange-red after grinding with a spatula. All the ground samples can be recovered to its original color by heating at 80 °C over 5 min or fuming with solvents like DCM, ethanol, ethyl acetate etc. The changes in fluorescence color can be attributed to the phase transition between crystalline (order) state and amorphous (disorder) state according to the Powder XRD spectrum. At the molecular level, the extension of the conjugation length and the formation of excimers are confirmed to account for the color transition of CDPA-P and CDPA-E, respectively. In addition, CDPA-P exhibited AIE activity which was caused by the restricted rotation of the molecules in the crystal state.

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