80594-29-2 Usage
Chemical structure
A complex organic molecule with multiple functional groups and stereochemistry.
Stereochemistry
The compound has a specific arrangement of atoms in space, with the stereochemistry being (2R,4S,5R).
Functional groups
Contains a tetrahydro-furan ring, a hydroxyl group, a pyrimidinone ring, phenyl groups, and methoxy groups.
Pyrimidine derivative
The compound is derived from a pyrimidine-based molecule, which is a common structural motif in many biologically active compounds.
Potential pharmaceutical applications
The compound may have potential uses in the pharmaceutical industry due to its structural features and biological activity.
Further research needed
More research is required to determine the specific potential uses and effects of this chemical compound.
Molecular weight
Approximately 552.64 g/mol
Appearance
Likely a solid, with the exact appearance depending on the conditions of synthesis and purification.
Solubility
The solubility of the compound is not specified, but it may be soluble in organic solvents such as methanol or dimethyl sulfoxide (DMSO), based on its structure.
Check Digit Verification of cas no
The CAS Registry Mumber 80594-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80594-29:
(7*8)+(6*0)+(5*5)+(4*9)+(3*4)+(2*2)+(1*9)=142
142 % 10 = 2
So 80594-29-2 is a valid CAS Registry Number.
80594-29-2Relevant academic research and scientific papers
Chemical synthesis of oligonucleotides containing the (6-4) photoproduct at the thymine-cytosine site and its repair by (6-4) photolyase
Iwai, Shigenori,Mizukoshi, Toshimi,Hitomi, Kenichi,Todo, Takeshi
, p. 1325 - 1327 (2007/10/03)
A phosphoramidite building block of the T(6-4)C photoproduct was synthesized. One of the differences from T(6-4)T was formation of cytosine hydrates by UV irradiation, and the other was acylation of the amino function with the capping reagent. The capping
Functionalization of solid supports with N-unprotected deoxyribonucleosides
Wada, Takeshi,Mochizuki, Akira,Sato, Yuichi,Sekine, Mitsuo
, p. 5593 - 5596 (2007/10/03)
N-Unprotected deoxyribonucleotides were loaded to solid supports via a succinyl or an oxalyl linker. These solid supports were successfully used for oligonucleotide synthesis by the H-phosphonate method without N-protecting groups.
Studies on the chemical synthesis of oligonucleotides containing the (6- 4) photoproduct of thymine-cytosine and its repair by (6-4) photolyase
Mizukoshi, Toshimi,Hitomi, Kenichi,Todo, Takeshi,Iwai, Shigenori
, p. 10634 - 10642 (2007/10/03)
To prepare oligonucleotides containing the pyrimidine(6-4)pyrimidone photoproduct between thymine and cytosine, which is formed more efficiently than any counterpart at other dipyrimidine sites, a dimer building block of this photoproduct was synthesized.
