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5'-O-DMT-2'-TBDMS-Uridine - 99%, high purity , CAS No.81246-80-2

COA

Grade & Purity:

for molecular biology

≥98%

Cas Number: 81246-80-2
Molecular Weight: 660.84
PubChem CID: 11017778

In stock

Item Number

O651660

Grouped product items
SKU	Size	Availability	Price
O651660-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$29.90
O651660-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$59.90
O651660-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$199.90
O651660-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$699.90

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Basic Description

Synonyms	AKOS015999127 \| 2'-O-tert-Butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)uridine \| 2'-O-tertButyldimethylsilyl-5'-O-DMT-uridine \| J-700111 \| 3'-O-tert-Butyldimethylsilyl-5'-O-DMT-uridine \| DTXSID50451982 \| 1-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)m
Specifications & Purity	Suitable for molecular biology, ≥98%
Biochemical and Physiological Mechanisms	5'-O-DMT-2'-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis.
Stability And Storage	Store at -2-8 ℃ (24 months). Under Inert Atmosphere. Store in the dark.
Storage Temp	Store at 2-8°C,Protected from light,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Grade	for molecular biology
Product Description	5'-O-DMT-2'-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Triphenyl compounds

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Triphenyl compounds
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Triphenyl compounds
Alternative Parents	Pyrimidine nucleosides Glycosylamines Pentoses Benzylethers Anisoles Phenoxy compounds Methoxybenzenes Alkyl aryl ethers Pyrimidones Hydropyrimidines Vinylogous amides Trialkylheterosilanes Heteroaromatic compounds Oxolanes Ureas Lactams Secondary alcohols Silyl ethers Azacyclic compounds Dialkyl ethers Organic metalloid salts Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Triphenyl compound - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzylether - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Pyrimidine - Vinylogous amide - Trialkylheterosilane - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Silyl ether - Lactam - Organic metalloid salt - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Organoheterosilane - Oxacycle - Organic oxide - Alcohol - Organic nitrogen compound - Organosilicon compound - Organic oxygen compound - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[tert-butyl(dimethyl)silyl]oxy-4-hydroxyoxolan-2-yl]pyrimidine-2,4-dione
INCHI	InChI=1S/C36H44N2O8Si/c1-35(2,3)47(6,7)46-32-31(40)29(45-33(32)38-22-21-30(39)37-34(38)41)23-44-36(24-11-9-8-10-12-24,25-13-17-27(42-4)18-14-25)26-15-19-28(43-5)20-16-26/h8-22,29,31-33,40H,23H2,1-7H3,(H,37,39,41)/t29-,31-,32-,33-/m1/s1
InChIKey	KVHQIELPHWJPSY-WXQJYUTRSA-N
Smiles	CC(C)(C)[Si](C)(C)OC1C(C(OC1N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)O
Isomeric SMILES	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)O
Molecular Weight	660.84

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Solubility	DMSO : 100 mg/mL (151.32 mM; Need ultrasonic)
Sensitivity	Light & Moisture & Air sensitive
Molecular Weight	660.800 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	12
Exact Mass	660.287 Da
Monoisotopic Mass	660.287 Da
Topological Polar Surface Area	116.000 Å²
Heavy Atom Count	47
Formal Charge	0
Complexity	1070.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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