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Trimethylsilanol-d1, also known as (trimethylsilyl)oxy-d1, is a deuterated form of trimethylsilanol, an organosilicon compound. It is a colorless liquid with a molecular formula of C3D9OSi and a molar mass of approximately 89.2 g/mol. trimethylsilanol-d1 is commonly used as a reagent in organic synthesis, particularly in the preparation of deuterated compounds, and as a protecting group in the synthesis of various organic molecules. Trimethylsilanol-d1 is also utilized in the study of reaction mechanisms and as a reference material in spectroscopic analysis. Its deuterated nature makes it a valuable tool for researchers to investigate the effects of isotopic substitution on chemical reactions and properties.

18026-73-8

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18026-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18026-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,2 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18026-73:
(7*1)+(6*8)+(5*0)+(4*2)+(3*6)+(2*7)+(1*3)=98
98 % 10 = 8
So 18026-73-8 is a valid CAS Registry Number.

18026-73-8Downstream Products

18026-73-8Relevant academic research and scientific papers

Silver-promoted desilylation catalyzed by ortho- and allosteric cucurbiturils

Lu, Xiaoyong,Masson, Eric

supporting information; experimental part, p. 2310 - 2313 (2010/08/04)

Cucurbit[6]-, [7]-, and [8]uril can catalyze the silver(I)-promoted desilylation of trimethylsilylalkynyl-containing pseudorotaxanes by stabilizing a key π-alkynyl silver intermediate through favorable interactions between the metallic cation and the cavi

Catalytic asymmetric Mannich-type reactions activated by ZnF2 chiral diamine in aqueous media

Hamada, Tomoaki,Manabe, Kei,Kobayashi, Shu

, p. 1205 - 1215 (2007/10/03)

Catalytic asymmetric Mannich-type reactions of an α-hydrazono ester with silicon enolates in aqueous media have been developed by using ZnF 2 and chiral diamines as catalysts. In these reactions, both Zn 2+ and a fluoride anion were necessary to achieve high yields and enantioselectivities. suggesting a double activation mechanism, in which Zn 2+ activates the α-hydrazono ester and the fluoride anion simultaneously activates the silicon enolate. When chiral diamine ligands bearing methoxy-substituted aromatic rings were employed, the reactions in aqueous THF were markedly accelerated. Furthermore, the use of these diamines facilitated the asymmetric Mannich-type reactions in water without any organic cosolvents. It is noteworthy that either syn or anti adducts were stereospecifically obtained from (E) or (Z)-silicon enolates, respectively. Interestingly, these reactions proceeded smoothly only in the presence of water. On the basis of several experimental results, it can be concluded that the reaction mechanism is likely to be a fluoride-catalyzed one, in which the ZnF2 chiral diamine complex is regenerated from the Me3SiF formed during the reaction.

Preparation of a new class of cleavable surfactants based on the silicon-carbon bond

Noronha, Glenn,Nguyen, Khanhlinh T.

, p. 4935 - 4938 (2007/10/03)

The ability of silicon to direct electrophiles to the ipso-position is used in developing a new class of cleavable amphiphiles containing an acid labile silicon-carbon (aromatic) bond. The synthesis of these amphiphiles is carried out in four steps to yie

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