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Triphenyl-thiophen-2-ylmethylene-λ5-phosphane is a complex organic compound characterized by its unique structure, which features a phosphorus atom bonded to three phenyl groups and a thiophene-2-ylmethylene group. triphenyl-thiophen-2-ylmethylene-λ5-phosphane is of interest in the field of organophosphorus chemistry, where it may be studied for its potential applications in materials science, as a ligand in coordination chemistry, or as a precursor in the synthesis of more complex molecules. The presence of the thiophene ring introduces unique electronic properties that can influence the compound's reactivity and stability. The compound's name reflects its structure, with "triphenyl" indicating the three phenyl groups attached to the phosphorus, "thiophen-2-ylmethylene" specifying the thiophene-based moiety, and "λ5-phosphane" denoting the phosphorus atom's involvement in the compound's structure.

41443-79-2

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41443-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41443-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41443-79:
(7*4)+(6*1)+(5*4)+(4*4)+(3*3)+(2*7)+(1*9)=102
102 % 10 = 2
So 41443-79-2 is a valid CAS Registry Number.

41443-79-2Relevant academic research and scientific papers

Synthesis and nonlinear optical absorption properties of two new conjugated ferrocene-bridge-pyridinium compounds

Yang, Fan,Xu, Xiu-Ling,Gong, Yong-Hua,Qiu, Wen-Wei,Sun, Zhen-Rong,Zhou, Jin-Wei,Audebert, Pierre,Tang, Jie

, p. 9188 - 9194 (2008/02/10)

Two electron donor-π-acceptor (D-π-A) chromospheres, with ferrocene as the electron donor and pyridinium as the electron acceptor, were synthesized. The nonlinear optical absorption (NOA) properties in the solution state were investigated by the Z-scan technique. Both compounds exhibited reverse saturable absorption (RSA) and optical limiting effect under nanosecond pulse irradiation.

Enzymatic desymmetrization of 2-amino-2-methyl-1,3-propanediol: Asymmetric synthesis of (S)-N-Boc-N,O-isopropylidene-α-methylserinal and (4R)-methyl-4-[2-(thiophen-2-yl)ethyl]oxazolidin-2-one

Tsuji, Takashi,Iio, Yukiko,Takemoto, Toshiyasu,Nishi, Takahide

, p. 3139 - 3142 (2007/10/03)

We report herein, the novel enzymatic desymmetrization of 2-tert-butoxycarbonylamino-2-methyl-1,3-propanediol 1. This method makes it possible to prepare (S)-N-Boc-N,O-isopropylidene-α-methylserinal 3, which is a chiral building block for the synthesis of a variety of α-substituted alanine derivatives. Moreover, optically active (4R)-methyl-4-[2-(thiophen-2- yl)ethyl]oxazolidin-2-one 4, one of the key intermediates in the synthesis of a novel immunosuppressant, has been prepared by this methodology.

A FACILE SYNTHESIS OF PERFLUORO- AND POLYFLUORO-ALKYL THIENYL ACETYLENES

Xin, Yuankang,Wu, Xiaohong,Shen, Yanchang

, p. 15 - 22 (2007/10/02)

Perfluro- and polyfluoro-alkyl thienyl acetylenes were conveniently prepared by the following reaction sequence: Thienylmethylenetriphenylphoshorane (generated from the corresponding chloride and phenyllithium without isolation) was acylated by the additi

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