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Home Other Building Blocks 2',3'-O-Isopropylideneuridine

2',3'-O-Isopropylideneuridine

CAS No.:
362-43-6
Catalog Number:
AG003FL4
Molecular Formula:
C12H16N2O6
Molecular Weight:
284.2652
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$82
- +
100g
98%
In Stock USA
United States
$300
- +
Product Description
Catalog Number:
AG003FL4
Chemical Name:
2',3'-O-Isopropylideneuridine
CAS Number:
362-43-6
Molecular Formula:
C12H16N2O6
Molecular Weight:
284.2652
MDL Number:
MFCD00034509
IUPAC Name:
1-[(3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]pyrimidine-2,4-dione
InChI:
InChI=1S/C12H16N2O6/c1-12(2)19-8-6(5-15)18-10(9(8)20-12)14-4-3-7(16)13-11(14)17/h3-4,6,8-10,15H,5H2,1-2H3,(H,13,16,17)/t6-,8-,9-,10-/m1/s1
InChI Key:
GFDUSNQQMOENLR-PEBGCTIMSA-N
SMILES:
OC[C@H]1O[C@H]([C@H]2[C@@H]1OC(O2)(C)C)n1ccc(=O)[nH]c1=O
EC Number:
206-647-7
Properties
Complexity:
477  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0
Exact Mass:
284.101g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
284.268g/mol
Monoisotopic Mass:
284.101g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
97.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.3  
Literature
Title Journal
5'-Uridyl derivatives of N-glycosyl allophanic acid and biuret. Carbohydrate research 20100111
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Synthesis of N3-substituted uridine and related pyrimidine nucleosides and their antinociceptive effects in mice. Chemical & pharmaceutical bulletin 20050301
Sugar-modified conjugated diene analogues of adenosine and uridine: synthesis, interaction with S-adenosyl-L-homocysteine hydrolase, and antiviral and cytostatic effects. Journal of medicinal chemistry 20020606
Properties