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123956-65-0

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  • N-(1-((2R,3R,4S,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-3-hydroxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide

    Cas No: 123956-65-0

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123956-65-0 Usage

General Description

3'-O-t-ButyldiMethylsilyl-5'-O-(4,4'-diMethoxytrityl)-N4-acetyl cytidine is a specialized chemical compound. The compound is known for its intricate structure and complex way of formation. It belongs to the group of silyl ethers, which are protective agents used extensively in organic synthesis. Additionally, it also consists of the 4,4'-dimethoxytrityl group, which is used for protecting hydroxyl groups in DNA synthesis as well as the N4-acetyl group indicating the cytidine derivative. Its name suggests that it is typically used in the protection and synthesis of various nucleosides and can be used in the study of genetics and biochemistry. The properties and the use of 3'-O-t-ButyldiMethylsilyl-5'-O-(4,4'-diMethoxytrityl)-N4-acetyl cytidine largely depend on its chemical structure.

Check Digit Verification of cas no

The CAS Registry Mumber 123956-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,5 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123956-65:
(8*1)+(7*2)+(6*3)+(5*9)+(4*5)+(3*6)+(2*6)+(1*5)=140
140 % 10 = 0
So 123956-65-0 is a valid CAS Registry Number.

123956-65-0Relevant articles and documents

The synthesis of allyl- and allyloxycarbonyl-protected RNA phosphoramidites. Useful reagents for solid-phase synthesis of RNAs with base-labile modifications

Bogdan, Felicia M.,Chow, Christine S.

, p. 1897 - 1900 (2007/10/03)

The synthesis of allyl- and allyloxycarbonyl (AOC)-protected RNA phosphoramidites is reported. The use of allyl and AOC groups allows the chemistry of solid-phase RNA synthesis to be expanded to include base-labile modified nucleosides, such as acetylcytidine. The allyl- and AOC-protective chemistry can be further expanded for the construction of RNAs on solid supports and affinity columns.

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