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Benzenesulfonic acid, 2,2-dimethyl-1-(trimethylsilyl)hydrazide is a complex organic compound with the chemical formula C10H22N2O2SSi. It is a derivative of benzenesulfonic acid, featuring a hydrazide group attached to the benzene ring, and a trimethylsilyl group connected to the nitrogen atom of the hydrazide. Benzenesulfonic acid, 2,2-dimethyl-1-(trimethylsilyl)hydrazide is known for its unique chemical properties, which make it useful in various applications, such as in the synthesis of pharmaceuticals and as a reagent in organic chemistry. Its structure provides a balance between the acidic properties of the benzenesulfonic acid and the nucleophilic characteristics of the hydrazide, while the trimethylsilyl group offers steric protection and can influence the reactivity of the molecule.

89902-35-2

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89902-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89902-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,0 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89902-35:
(7*8)+(6*9)+(5*9)+(4*0)+(3*2)+(2*3)+(1*5)=172
172 % 10 = 2
So 89902-35-2 is a valid CAS Registry Number.

89902-35-2Downstream Products

89902-35-2Relevant academic research and scientific papers

Structure of Silylated Sulfonamides; a Silicon-29 Nuclear Magnetic Resonance Investigation

Iley, Jim,Bassindale, Alan R.,Patel, Pravin

, p. 77 - 80 (2007/10/02)

The structures of eighteen silylsulfonamides have been determined by 29Si n.m.r.The chemical shifts of the compounds were compared with those of model compounds.The N-silyl tautomer was the only isomer observed, except in cases where strongly electron-withdrawing groups (e.g.Cl, NMe2) were attached to nitrogen; in such cases the O-silyl tautomer dominates.The results have been rationalised in terms of the effect of substituents on the S-N ?-bond order.An estimate of the hitherto unmeasured S=N molar bond enthalpy as 325 kJ mol-1 was obtained.

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