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methyl 3-phenyl-2-(trimethylsilyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128059-56-3

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128059-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128059-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128059-56:
(8*1)+(7*2)+(6*8)+(5*0)+(4*5)+(3*9)+(2*5)+(1*6)=133
133 % 10 = 3
So 128059-56-3 is a valid CAS Registry Number.

128059-56-3Relevant academic research and scientific papers

Facile Isomerization of Trimethylsilyl Ketene Acetals to α-Trimethylsilyl Esters Catalyzed by Lanthanoid Trifluoromethanesulfonates

Makioka, Yoshikazu,Taniguchi, Yuki,Takaki, Ken,Fujiwara, Yuzo

, p. 645 - 648 (1994)

Migration of trimethylsilyl group from oxygen to α-carbon in silyl ketene acetals is effectively catalyzed by lanthanoid triflates under mild conditions.Scope and limitation of this rearrangement are presented.

Michael addition of methyl 2-(trimethysily)propenoate with organomagnesiums or organolithiums leading to 1:1 and / or 2:1 adducts and subsequent peterson olefination by condensation with carbonyl compounds

Tanaka,Kanemasa,Ninomiya,Tsuge

, p. 466 - 475 (2007/10/02)

Michael addition of methyl 2-(trimethylsilyl)propenoate with organomagnesiums or organolithiums leads to 1:1 and/or 1:2 adduct anions which can be utilized in the subsequent step of Peterson olefination with carbonyl compounds. The 1:1/1:2 ratio depends u

Cleavage of Carbon-Carbon Bonds with High Stereochemical Control. 6. Asymmetric Synthesis of Chiral C-Centered Organosilanes by Haller-Bauer Cleavage of Optically Active, Nonenolizable α-Silyl Phenyl Ketones

Gilday, John P.,Gallucci, Judith C.,Paquette, Leo A.

, p. 1399 - 1408 (2007/10/02)

Sequential alkylation and methylation of l-menthyl ester 10 provides diastereomeric mixtures in which 12 is slighthly enhanced over 13.Conversely, C-silation and alkylation of propionate ester 11 delivers 13 in excess.In either cause, a single chromatogra

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