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3-[[(2R,3S,5R)-3-Hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-bis-(4-methoxy-phenyl)-methyl]-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154965-35-2

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154965-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154965-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,9,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154965-35:
(8*1)+(7*5)+(6*4)+(5*9)+(4*6)+(3*5)+(2*3)+(1*5)=162
162 % 10 = 2
So 154965-35-2 is a valid CAS Registry Number.

154965-35-2Downstream Products

154965-35-2Relevant academic research and scientific papers

Heterobifunctional Trityl Derivatives as Linking Reagents for the Recovery of Nucleic Acids after Labeling and Immobilization

Leikauf, Eckart,Barnekow, Frank,Koester, Hubert

, p. 3793 - 3802 (2007/10/02)

The synthesis of two heterobifunctional 4,4'-dimethoxytrityl derivatives carrying a N-hydroxysuccinic acid group as active ester in para 5a or meta position 5b is described.While 5a has been synthesized previously via six steps a novel and more efficient four step synthesis for both compounds is introduced here.The meta compound 5b provides for a more acid labile trityl ether linkage compared to the para derivative 5a.Using these compounds as linking agents biopolymers in particular nucleic acids can easily be recovered after labeling or immobilization by treatment with a mild acid such as 80percent aqueous acetic acid.

New 5′-hydroxyl protecting groups for rapid internucleotide bond formation

Sekine, Mitsuo,Mori, Toshiya,Wada, Takeshi

, p. 8289 - 8292 (2007/10/02)

A variety of 5′-hydroxyl protecting groups having catalytic sites for internucleotidic bond formation have been studied. Among them, a modified dimethoxytrityl group having an imidazolylethylcarbamoyl substituent has proved to be highly effective and superior to die IDTr group previously known.

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