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2,2,4-Trimethyl-2-germa-1,3-thiazolidine is a chemical compound with the molecular formula C6H14GeNS. It is a derivative of 1,3-thiazolidine, which is a heterocyclic compound containing a sulfur atom and a nitrogen atom. The presence of three methyl groups (CH3) and a germyl group (GeH3) in the molecule gives it unique properties. 2,2,4-trimethyl-2-germa-1,3-thiazolidine is of interest in the field of organometallic chemistry, particularly in the study of germanium-containing compounds and their potential applications in various chemical reactions and materials science. Its structure and reactivity make it a subject of research for understanding the behavior of heavier group 14 elements in organic synthesis and their potential use in pharmaceuticals or other industrial applications.

86553-79-9

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86553-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86553-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86553-79:
(7*8)+(6*6)+(5*5)+(4*5)+(3*3)+(2*7)+(1*9)=169
169 % 10 = 9
So 86553-79-9 is a valid CAS Registry Number.

86553-79-9Downstream Products

86553-79-9Relevant academic research and scientific papers

GERMANONES ET GERMATHIONES: REACTIVITE VIS-A-VIS DE PETITS CYCLES ORGANIQUES

Barrau, Jacques,Rima, Ghassoub,Lavayssiere, Helene,Dousse, Gabriel,Satge, Jacques

, p. 227 - 242 (2007/10/02)

Dialcoylgermanones and dialcoylgermathiones are generated from various germa-heterocyclic precursors and dimeric or trimeric forms (R2GeO)2 and (R2GeS)3.These species (X = O, S) react with various three- or four-membered rings (n = 2, Y = O, S, NR, CHCN; n = 3, Y = O, S) to lead to the germaheterocycles (X = O, S).Cyclogermathianes (R2GeS)3 lead very easily, by thermic and catalytic dissociation to the germathiones .Basic solvent (Et3N, HMPA) and catalysts induce these dissociations.Mechanism and stereochemistry ofinsertion reactions of these transient species (X = O, S) into oxirane rings are established from cis- and trans-butene oxides.The formation of germanium hexacoordinated intermediate complex can explain the observed stereoselectivity.With germathiones the stereoselectivity derives from the strong nucleophilic activity of these species.

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