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123883-51-2

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123883-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123883-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,8 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123883-51:
(8*1)+(7*2)+(6*3)+(5*8)+(4*8)+(3*3)+(2*5)+(1*1)=132
132 % 10 = 2
So 123883-51-2 is a valid CAS Registry Number.

123883-51-2Relevant articles and documents

Glucose-Responsive Hybrid Nanoassemblies in Aqueous Solutions: Ordered Phenylboronic Acid within Intermixed Poly(4-hydroxystyrene)-block-poly(ethylene oxide) Block Copolymer

Matuszewska, Alicja,Uchman, Mariusz,Adamczyk-Wo?niak, Agnieszka,Sporzyński, Andrzej,Pispas, Stergios,Ková?ik, Lubomír,?těpánek, Miroslav

, p. 3731 - 3739 (2015)

Coassembly behavior of the double hydrophilic block copolymer poly(4-hydroxystyrene)-block-poly(ethylene oxide) (PHOS-PEO) with three amphiphilic phenylboronic acids (PBA) differing in hydrophobicity, 4-dodecyloxyphenylboronic acid (C12), 4-octyloxyphenyl

Enthalpy-entropy compensation combined with cohesive free-energy densities for tuning the melting temperatures of cyanobiphenyl derivatives

Dutronc, Thibault,Terazzi, Emmanuel,Guenee, Laure,Buchwalder, Kerry-Lee,Spoerri, Aurore,Emery, Daniel,Mareda, Jiri,Floquet, Sebastien,Piguet, Claude

, p. 8447 - 8456 (2013)

This work illustrates how minor structural perturbations produced by methylation of 4′-(dodecyloxy)-4-cyanobiphenyl leads to enthalpy-entropy compensation for their melting processes, a trend which can be analyzed within the frame of a simple intermolecular cohesive model. The transformation of the melting thermodynamic parameters collected at variable temperatures into cohesive free-energy densities expressed at a common reference temperature results in a novel linear correlation, from which melting temperatures can be simply predicted from molecular volumes. In tune with temperature! The transformation of the melting thermodynamic parameters into cohesive free-energy densities (CFED) for 4′-(n-oxy)-i′-methyl-j-methyl-4-cyanobiphenyl (CnLi′,j) provides a novel linear correlation for predicting melting temperatures in a simple way. Copyright

Semi-fluorinated p-terphenyl liquid crystals

Valdés-Pech, Moisés Alberto,Larios-López, Leticia,Rodríguez-González, Rosa Julia,Felix-Serrano, Isaura,Trejo-Carbajal, Nayely,Navarro-Rodríguez, Dámaso

, p. 42 - 50 (2019)

p-Terphenyls carrying two or four fluorine atoms in the central ring were synthesized via Suzuki-Miyaura cross-coupling reaction using phenylboronic acids and fluorinated dibromobenzenes. By calorimetric and X-ray diffraction analyses it was found that th

COMPOUND, DETECTION MATERIAL AND DETECTION METHOD OF SUGAR COMPOUND USING THE SAME

-

Paragraph 0084; 0085, (2020/02/22)

PROBLEM TO BE SOLVED: To provide a novel compound suitable for detection of a sugar compound, and detection means of the sugar compound using the same. SOLUTION: There is provided a compound represented by the general formula (A1) or (B1). Ar1 is a substituent and/or an aromatic ring which may have a hetero group in a ring; each Ar2 each independently is an aromatic ring which may have a substituent, Ar3 is an aromatic ring which has at least one -B(OH)2 and may have a substituent; R1 is H or a C1 to 20 alkyl group or an alkyloxy group which may have a hetero atom in a middle of a carbon chain; n is an integer of 1 to 5; and a bond represented by a combination of a double bond and a dash line each independently is a double bond or a triple bond. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Novel AuI polyynes and their high optical power limiting performances both in solution and in prototype devices

Tian, Zhuanzhuan,Yang, Xiaolong,Liu, Boao,Zhao, Jiang,Zhong, Daokun,Wu, Yong,Zhou, Guijiang,Wong, Wai-Yeung

supporting information, p. 6023 - 6032 (2018/06/15)

Three novel AuI polyynes have been prepared in high yield by copolymerization between an AuI complex precursor and different ethynyl aromatic ligands. The investigation of their photophysical behavior has indicated that forming polyynes through polymerization not only maintains the high transparency of the corresponding AuI polyynes similar to those of their corresponding small molecular AuI acetylides, but also effectively enhances their triplet (T1) emission ability. Critically, owing to their enhanced T1 emission ability, all the AuI polyynes exhibit a stronger optical power limiting (OPL) ability against a 532 nm laser than the corresponding small molecular AuI acetylides. The AuI polyynes based on fluorene and triphenylamine ligands show even better OPL performance than the state-of-the-art OPL material C60, indicating their great potential in the field of laser protection. More importantly, in a prototype OPL device made by doping the fluorene-based AuI polyyne into a polystyrene (PS) solid matrix, substantially improved OPL activity has been observed compared with that in the solution, demonstrating its great potential for practical application. All these results have provided a new strategy to achieve a balance between high OPL activity and good transparency for OPL materials, representing a valuable attempt towards developing new OPL materials with high performance to cope with the key problems in the field of nonlinear optics.

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