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5'-O-(4,4'-dimethoxytrityl)thymidine 3'-O-[2-(trimethylsilyl)ethyl] diisopropylphosphoramidite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173653-35-5

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173653-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173653-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,6,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173653-35:
(8*1)+(7*7)+(6*3)+(5*6)+(4*5)+(3*3)+(2*3)+(1*5)=145
145 % 10 = 5
So 173653-35-5 is a valid CAS Registry Number.

173653-35-5Downstream Products

173653-35-5Relevant academic research and scientific papers

Fluoride-labile protecting groups for the synthesis of base-sensitive methyl-SATE oligonucleotide prodrugs

Guerlavais-Dagland, Typhaine,Meyer, Albert,Imbach, Jean-Louis,Morvan, Francois

, p. 2327 - 2335 (2003)

Base-sensitive methyl-SATE oligonucleotide prodrugs (prooligos) were synthesized using fluoride-labile protection groups on the nucleobases and on certain internucleosidic phosphate linkages. The combination of [(tert-butyl)(diphenyl)silyloxymethyl]benzoy

Silyl protecting groups for oligonucleotide synthesis removed by a ZnBr2 treatment

Ferreira, Fernando,Morvan, Francois

, p. 1009 - 1013 (2007/10/03)

An oligonucleotide protected with N-(trimethylsilyloxycarbonyl) (Teoc) and P-(trimethylsilylethanol) (Tse) groups was synthesized and deprotected by a single ZnBr2 treatment. Finally it was released from the solid support by cleavage of a disul

Lewis acid deprotection of silyl-protected oligonucleotides and base-sensitive oligonucleotide analogues

Ferreira, Fernando,Vasseur, Jean-Jacques,Morvan, Fran?ois

, p. 6287 - 6290 (2007/10/03)

a- a- a- Oligonucleotides protected with N-(trimethylsilylethoxycarbonyl) (Teoc) and P-(trimethylsilylethanol) (Tse) groups were synthesized and deprotected by a single ZnBr2 treatment. Teoc group stabilized dA against depurination. This strategy was applied to the synthesis of base-sensitive oligonucleotide prodrugs bearing S-acetyl-2-thioethyl (Sate) phosphotriesters.

Phosphorothioate: β-Fragmentierung gegen β-Silicium-Effekt

Krotz, Achim H.,Wheeler, Patrick,Ravikumar, Vasulinga T.

, p. 2584 - 2587 (2007/10/03)

Keywords: Antisense-Oligonucleotide, Nachbargruppeneffekte, Nucleotide, Phosphorverbindungen, Umlagerungen

2-(Trimethylsilyl)ethyl as a Phosphate Protecting Group in Oligonucleotide Synthesis

Wada, Takeshi,Sekine, Mitsuo

, p. 757 - 760 (2007/10/02)

The 2-(trimethylsilyl)ethyl (TSE) group was found to be effective as a protecting group for the internucleotidic phosphate in oligonucleotide synthesis.Phosphoramidite building blocks having the TSE group were prepared in good yields.In the case of deoxyg

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