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Acetic acid, [[tris(1-methylethyl)silyl]oxy]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192758-34-2

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192758-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192758-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,7,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 192758-34:
(8*1)+(7*9)+(6*2)+(5*7)+(4*5)+(3*8)+(2*3)+(1*4)=172
172 % 10 = 2
So 192758-34-2 is a valid CAS Registry Number.

192758-34-2Downstream Products

192758-34-2Relevant academic research and scientific papers

Fluorinated taxane compound, preparation method therefor and application of fluorinated taxane compound

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Paragraph 0048; 0050; 0055-0057, (2019/08/30)

The invention discloses a fluorinated taxane compound, a preparation method therefor and an application of the fluorinated taxane compound. The compound has a structural general formula represented bya formula I. Proven by pharmacological experiments, compared with paclitaxel, a series of fluorinated taxane derivatives synthesized by the method have cytotoxicity superior to that of the paclitaxelto a multidrug-resistant human mammary cancer cell line MCF-7/Adr and an ovarian cancer cell line NCI/Adr and represent cytotoxicity superior to that of the paclitaxel to a colon cancer cell line HCT-116 with overexpressed neoplasm stem cells.

An inexpensive carbohydrate derivative used as a chiral auxiliary in the synthesis of α-hydroxy carboxylic acids

Yu, Hongwu,Ballard, C.Eric,Boyle, Paul D,Wang, Binghe

, p. 7663 - 7679 (2007/10/03)

Protected α-hydroxy carboxylic acids were synthesized in moderate yield and high diastereoselectivity by alkylation of glycolate (α-hydroxy acetate) enolates using a D-fructose-derived chiral auxiliary. The new chiral center was assigned the R configuration based on comparisons of optical rotations and on one crystal structure analysis. This alkylation methodology is compatible with several hydroxyl protecting groups. The free hydroxy acids were obtained upon removal of the protecting group from the hydroxyl functionality followed by saponification.

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