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131368-48-4

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131368-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131368-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,6 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131368-48:
(8*1)+(7*3)+(6*1)+(5*3)+(4*6)+(3*8)+(2*4)+(1*8)=114
114 % 10 = 4
So 131368-48-4 is a valid CAS Registry Number.

131368-48-4Downstream Products

131368-48-4Relevant academic research and scientific papers

Steady-state photolysis of dimesitylbis(trimethylsilyl)germane

Hurni, Krysten L.,Baines, Kim M.

, p. 668 - 674 (2008/09/19)

The photolysis of dimesitylbis(trimethylsilyl)germane (3) in hexanes or THF, at low temperature, has been investigated as a potential method for the preparative-scale synthesis of tetramesityldigermene (5). A product mixture, consisting of hexamethyldisilane, mesitylene, 2-trimethylsilylmesitylene (7), a new germacyclobutene (8), and an unidentified polymer, was obtained. No evidence for the formation of tetramesityldigermene (5) was observed.

Organogermanium reactive intermediates. The direct detection and characterization of transient germylenes and digermenes in solution

Leigh, William J.,Harrington, Cameron R.,Vargas-Baca, Ignacio

, p. 16105 - 16116 (2007/10/03)

Diphenylgermylene (Ph2Ge) and its Ge=Ge doubly bonded dimer, tetraphenyldigermene (6a), have been characterized directly in solution for the first time by laser flash photolysis methods. The germylene is formed via (formal) cheletropic photocycloreversion of 3,4-dimethyl-1,1- diphenylgermacyclopent-3-ene (4a), which is shown to proceed in high chemical (>95%) and quantum yield (Φ = 0.62) by steady-state trapping experiments with methanol, acetic acid, isoprene, and triethylsilane. Flash photolysis of 4a in dry deoxygenated hexane at 23°C leads to the prompt formation of a transient assigned to Ph2Ge (∈max = 500 nm; ∈max = 1650 M-1 cm-1), which decays with second-order kinetics (τ ≈ 3 μs), with the concomitant growth of a second transient species that is assigned to digermene 6a (τ ≈ 40 μs; λmax = 440 nm). Analogous results are obtained from 1,1-dimesityl- and 1,1-dimethyl-3,4-dimethylgermacyclopent-3-ene (4b and 4c, respectively), which afford Mes2Ge (τ = 20 μs; λmax = 560 nm) and Me2Ge (τ ≈ 2 μs; λs; λmax = 480 nm), respectively, as well as the corresponding digermenes, tetramesityl- (6b; λmax = 410 nm) and tetramethyldigermene (6c; λmax = 370 nm). The results for the mesityl compound are compared to the analogous ones from laser flash photolysis of the known Mes2Ge/6b precursor, hexamesitylcyclotrigermane. The spectra of the three germylenes and two of the digermenes are in excellent agreement with calculated spectra, derived from time-dependent DFT calculations. Absolute rate constants for dimerization of Ph2Ge and Mes2Ge and for their reaction with n-butylamine and acetic acid in hexane at 23°C are also reported.

From a germene to a transient germirane

Lazraq, M.,Escudie, J.,Couret, C.,Satge, J.,Soufiaoui, M.

, p. 1 - 6 (2007/10/02)

Reaction of dimesityl(fluorenylidene)germene, 1, with diazomethane leads, depending on the expetimental conditions, to the germapyrazoline 3 or 4.Thermal decomposition of 4 gives an unstable germirane 14, which was identified from its deco

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