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O-trimethylsilyl 4-methylbenzenecarbotelluroate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174018-12-3

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174018-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174018-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 174018-12:
(8*1)+(7*7)+(6*4)+(5*0)+(4*1)+(3*8)+(2*1)+(1*2)=113
113 % 10 = 3
So 174018-12-3 is a valid CAS Registry Number.

174018-12-3Upstream product

174018-12-3Downstream Products

174018-12-3Relevant academic research and scientific papers

A Facile Preparation of Cesium Tellurocarboxylates. The First X-Ray Structural Analysis of a Tellurocarboxylic Acid Alkali Matal Salt

Kawahara, Yasuyuki,Kato, Shinzi,Kanda, Takahiro,Murai, Toshiaki

, p. 87 - 88 (1995)

Crystalline cesium tellurocarboxylates have been isolated from the reaction of O-trimethylsilyl tellurocarboxylates with cesium fluoride and characterized by X-ray crystallographic analysis which showed a C-Te single bond (2.107 Angstroem) and the possibi

Synthesis of Rubidium and Cesium Tellurocarboxylates and an X-Ray Structural Analysis of Heavy Alkali Metal Monochalcogenocarboxylates

Kawahara, Yasuyuki,Kato, Shinzi,Kanda, Takahiro,Murai, Toshiaki,Ebihara, Masahiro

, p. 3507 - 3518 (2007/10/03)

A series of rubidium and cesium tellurocarboxylates (2 and 3) were synthesized from the reaction of O-trimethylsilyl tellurocarboxylates (1) with rubidium and cesium fluorides in moderate isolated yields and characterized by 1H, 13C, and 125Te NMR spectroscopy and X-ray diffraction.The carbon-oxygen distance of the tellurocarboxyl group of crystalline cesium 2-methoxybenzenecarbotelluroate (3f) showed a typical value of the carbon-oxygen double bond.The crystal packing of 3f shows the possibility of an interaction between the cesium cation and the aromatic ring carbon.The thio- and selenocarboxyl groups of the corresponding sulfur and selenium isologues (4 and 5) also indicate a double bond between the carbon and oxygen, respectively.The salts ( 2 and 3) readily react with iodomethane to afford the corresponding Te-methyl tellurocarboxylates in good yields.The reaction between 3 and tetramethylammonium chloride was found to give a novel quaternary ammonium salt (8) of tellurocarboxylic acid, where the dihedral angle between benzene ring and the tellurocarboxyl group of 8 is ca. 90 deg.Crystallographic data for 3f, 4, 5, and 8 are as follows. 3f: P21/n, a=7.182(2), b=12.161(5), c=12.151(3) Angstroem, β=92.57(2) deg, V=1060.2(6) Angstroem3, dcalcd=2.479 g cm-3, Z=4, R=0.035, Rw=0.043. 4: Pbca, a=8.995(2), b=29.936(2), c=7.291(1) Angstroem, V=1963.3(5) Angstroem3, dcalcd=2.030 g cm-3, Z=8, R=0.024, Rw=0.021. 5: Pbca, a=9.290(1), b=30.207(2), c=7.193(2) Angstroem, V=2018.5(3) Angstroem3, dcalcd=2.284 g cm-3, Z=8, R=0.029, Rw=0.020. 8: P212121, a=11.844(2), b=14.014(2), c=8.650(1) Angstroem, V=1435.8(3) Angstroem3, dcalcd=1.558 g cm-3, Z=4, R=0.044, Rw=0.047.

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