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ChemicalBook--->CAS DataBase List--->81246-80-2

81246-80-2

81246-80-2 Structure

81246-80-2 Structure
IdentificationBack Directory
[Name]

5'-O-DMT-2'-TBDMS-Uridine
[CAS]

81246-80-2
[Synonyms]

DMT-2'-O-TBDMS-Ur
5'-DMT-2'-TBDMS-rU
5'-O-DMT-2'-O-TBDMS-rU
5'-DMTr-2'-TBDMS-uridine
5'-O-DMT-2'-TBDMS-Uridine
5'-O-DMT-2'-O-TBDMS uridine
2'-O-TBDMS-5'-O-DMT-uridine
2'-O-tertButyldimethylsilyl-5'-O-DMT-uridine
5'-O-(4,4'-DiMethoxytrityl)-2'-O-t-butyldiMethylsilyl uridine
2'-O-tert-ButyldiMethylsilyl-5'-O-(4,4'-diMethoxytrityl)uridine
1-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)met...
Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-
1-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-((tert-butyldimethylsilyl)o
1-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-((tert-butyld methylsilyl)oxy)
1-((2R,3R,4R,5R)-5-((Bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)-3-((tert-butyldiMethylsilyl)oxy)-4-hydroxytetrahydrofuran-2-yl)pyriMidine-2,4(1H,3H)-dione
[EINECS(EC#)]

2017-001-1
[Molecular Formula]

C36H44N2O8Si
[MDL Number]

MFCD00135726
[MOL File]

81246-80-2.mol
[Molecular Weight]

660.83
Chemical PropertiesBack Directory
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

DMSO : 100 mg/mL (151.32 mM; Need ultrasonic)
[form ]

Solid
[pka]

9.39±0.10(Predicted)
[color ]

White to light yellow
[InChIKey]

KVHQIELPHWJPSY-WLVJKCSANA-N
[SMILES]

O(C(C1=CC=C(OC)C=C1)(C1=CC=C(OC)C=C1)C1=CC=CC=C1)C[C@H]1O[C@@H](N2C=CC(=O)NC2=O)[C@H](O[Si](C(C)(C)C)(C)C)[C@@H]1O |&1:25,27,36,45,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Uses]

5''-O-DMT-2''-TBDMS-Uridine (cas# 81246-80-2) is a nucleoside and has been used in the prepartion of pseudorotaxane architectures. It has also been able to undergo microwave-assisted phosphitylation in the preparation of nucleoside phosphoramidites.
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