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1003194-88-4

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1003194-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1003194-88-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,1,9 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1003194-88:
(9*1)+(8*0)+(7*0)+(6*3)+(5*1)+(4*9)+(3*4)+(2*8)+(1*8)=104
104 % 10 = 4
So 1003194-88-4 is a valid CAS Registry Number.

1003194-88-4Downstream Products

1003194-88-4Relevant articles and documents

Novel 1,2-dicarba-closo-dodecaborane(12) derivatives of selenium

Wrackmeyer, Bernd,Hernandez, Zureima Garcia,Kempe, Rhett,Herberhold, Max

, p. 239 - 246 (2007)

Lithiation of 1,2-dicarba-closo-dodecaborane(12) (1) followed by insertion of selenium into both C-Li bonds leads to the 1,2-diselenolato-1,2-dicarba- closo-dodecaborane(12) dianion (3), which is converted by oxidative coupling into the cyclic eight-membered bis(diselane) 4 with annellated carborane moieties. Oxidative addition of 4 to ethenebis(triphenylphosphane)platinum(0) gives the bis(triphenylphosphane)platinum(II) complex 7, which contains a chelating 1,2-diselenolato-1,2-dicarba-closo-dodecaborane(12) ligand, by symmetric cleavage of the eight-membered ring in 4 and displacement of ethene. The molecular structures of 4 and 7 were determined by X-ray analysis. The solution-state structures of the new compounds are supported by multinuclear NMR data (1H, 11B, 13C, 29Si, 31P, 77Se, 195Pt). Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

1,3,2-Diselenaphospholanes with an anellated dicarba-closo-dodecaborane(12) unit

Wrackmeyer, Bernd,Hernandez, Zureima Garcia,Kempe, Rhett,Herberhold, Max

, p. 851 - 857 (2008/10/09)

The reaction of the 1,2-diselenido-1,2-dicarba-closo-dodecaborane dianion (1) with dichloro(phenyl)phosphane affords the 1,3,2-diselenaphospholane (2) containing an anellated dicarba-closo-docecaborane(12) unit. The phospholane 2 was oxidised by reactions with the elements to the sulfide 3 and the selenide 4, and partial hydrolysis gave a selenophosphonic acid derivative 5 along with the bis(diselane) 6 and decomposition. The reaction of 2 with (ethene) bis(triphenylphosphane)platinum(0) displaces ethene and is accompanied by oxidative addition and rearrangement into the bis(triphenylphosphane) platinum(II) complex 9, in which the chelating unit is linked to platinum via Pt-Se and Pt-P(Se) bonds, a rare example of a metallophosphane selenide. The molecular structures of 2 and 3 were determined by X-ray analysis. The solution-state structures of the new compounds follow from consistent multinuclear magnetic resonance data (1H, 11B, 13C, 31P, 77Se, 195Pt NMR).

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