Uridine, 2'-O-[(1,1-dimethylethyl)dimethylsilyl]-|54925-71-2,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Uridine, 2'-O-[(1,1-dimethylethyl)dimethylsilyl]-

OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O[Si](C(C)(C)C)(C)C)n1ccc(=O)[nH]c1=O

Request for Quotation

Chemical Name:	Uridine, 2'-O-[(1,1-dimethylethyl)dimethylsilyl]-
CAS Number:	54925-71-2
Product Number:	AG00DJLV(AGN-PC-0OC5AN)
Synonyms:
MDL No:
Molecular Formula:	C15H26N2O6Si
Molecular Weight:	358.46224

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Properties

Storage:

2-8℃;

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

2'-TBDMS-rU is a highly versatile nucleoside derivative that finds wide applications in chemical synthesis. Its unique structural characteristics make it a valuable building block in the creation of diverse compounds for various purposes. In the realm of chemical synthesis, 2'-TBDMS-rU is commonly used as a key intermediate in the production of nucleic acid analogs, pharmaceuticals, and bioconjugates. By harnessing its reactivity and compatibility with numerous functional groups, researchers can efficiently introduce specific modifications into molecules, facilitating the development of novel materials and bioactive compounds. Additionally, its stability and solubility properties further enhance its utility in complex synthetic schemes, making it an indispensable tool in the construction of intricate molecular architectures.