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Oxazole, 2,2'-(1,2-phenylene)bis[4,5-dihydro-4-phenyl-, (4S,4'S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131380-82-0

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131380-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131380-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,8 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131380-82:
(8*1)+(7*3)+(6*1)+(5*3)+(4*8)+(3*0)+(2*8)+(1*2)=100
100 % 10 = 0
So 131380-82-0 is a valid CAS Registry Number.

131380-82-0Relevant academic research and scientific papers

New palladium-oxazoline complexes: Synthesis and evaluation of the optical properties and the catalytic power during the oxidation of textile dyes

Hassani, Rym,Jabli, Mahjoub,Kacem, Yakdhane,Marrot, Jrme,Prim, Damien,Hassine, Bchir Ben

, p. 1175 - 1186 (2015)

The present paper describes the synthesis of new palladium-oxazoline complexes in one step with good to high yields (68-95%). The oxazolines were prepared from enantiomerically pure α-aminoalcohols. The structures of the synthesized palladium complexes we

Synthesis of Optically Active Bis(2-oxazolines): Crystal Structure of a 1,2-Bis(2-oxazolinyl)benzene * ZnCl2 Complex

Bolm, Carsten,Weickhardt, Konrad,Zehnder, Margareta,Ranff, Tobias

, p. 1173 - 1180 (2007/10/02)

Dinitriles (5-7, 12, 13) react with enantiomerically pure β-amino alcohols (8-11, 17) under zinc chloride catalysis to give optically active C2-symmetric bis(oxazolines). 1,2-Bis(2-oxazolin-2-yl)benzenes 1a-e are obtained under mild reaction conditions. 1H-NMR spectroscopy indicates the formation of 1:1 complexes 23 of these compounds with ZnCl2.The energy required for a conformational interconversion of zinc dichloride complex 23e was determined by variable-temperature 1H-NMR studies.An X-ray structure analysis was performed with the substituted zinc dichloride complex 23a.

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