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1-Phenyl-4-(2-thienyl)-1,3-butadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52380-84-4

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52380-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52380-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52380-84:
(7*5)+(6*2)+(5*3)+(4*8)+(3*0)+(2*8)+(1*4)=114
114 % 10 = 4
So 52380-84-4 is a valid CAS Registry Number.

52380-84-4Downstream Products

52380-84-4Relevant academic research and scientific papers

Excited-state energy levels and photophysics of a short polyene 2-(4-phenyl-1,3-butadien-1-yl)thiophene

Itoh, Takao

, p. 40 - 46 (2016/04/05)

Emission, excitation and absorption spectra of a new and short polyene, 2-(4-phenyl-1,3-butadien-1-yl)thiophene (PBT), have been measured under different conditions by varying temperature and solvent and in the vapor phase, along with those of 2-(2-phenyl

Indium triflate catalyzed rearrangement of aryl-substituted cyclopropyl carbinols to 1,4-disubstituted 1,3-butadienes

Ranu, Brindaban C.,Banerjee, Subhash

, p. 3012 - 3015 (2007/10/03)

Aryl-substituted cyclopropyl carbinol derivatives undergo a facile stereoselective rearrangement catalyzed by In(OTf)3 in dichloromethane under sonication to produce the substituted conjugated all-trans-butadienes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Catalysis by ionic liquids: Cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions

Ranu, Brindaban C.,Banerjee, Subhash,Das, Arijit

, p. 881 - 884 (2007/10/03)

Aryl substituted cyclopropyl carbinol derivatives undergo stereoselective rearrangements catalyzed by the ionic liquid, 1-methyl-3-pentylimidazolium bromide, under sonication, without any organic solvent, to produce the substituted conjugated all-trans-butadienes.

THE ONE-POT PALLADIUM CATALYZED WITTIG REACTION WITH ALLYLIC ALCOHOLS. SCOPE AND LIMITATIONS

Moreno-Manas, M.,Ortuno, R. M.,Prat, M.,Galan, M. A.

, p. 1003 - 1014 (2007/10/02)

Some allylic alcohols react with aldehydes and triphenylphosphine in a one-pot formal Wittig reaction under Pd0 catalysis.The method has been extended to cinnamyl alcohol, 1, 2-methyl-2-propen-1-ol, 7, and 3-buten-2-ol, 11, and to heterocyclic aldehydes.

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