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4-methoxy-1-(2,3,5-tri-O-benzoylpentofuranosyl)pyrimidin-2(1H)-one is a complex organic compound with a molecular formula of C31H25N3O9. It is a derivative of pyrimidin-2(1H)-one, featuring a 4-methoxy group and a pentofuranosyl moiety, which is substituted with three benzoyl groups at the 2, 3, and 5 positions. 4-methoxy-1-(2,3,5-tri-O-benzoylpentofuranosyl)pyrimidin-2(1H)-one is of interest in the field of organic chemistry and may have potential applications in pharmaceutical research due to its unique structure and functional groups. The presence of the benzoyl groups can influence the compound's reactivity and stability, while the methoxy group and the pyrimidin-2(1H)-one core contribute to its potential biological activity.

2873-31-6

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2873-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2873-31-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2873-31:
(6*2)+(5*8)+(4*7)+(3*3)+(2*3)+(1*1)=96
96 % 10 = 6
So 2873-31-6 is a valid CAS Registry Number.

2873-31-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-1-(tri-O-benzoyl-β-D-ribofuranosyl)-1H-pyrimidin-2-one

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:2873-31-6 SDS

2873-31-6Relevant academic research and scientific papers

Incorporation of methylated pyrimidine analogues into RNA

Vyle, Joseph S.,Young, Karen J.,Grasby, Jane A.

, p. 5093 - 5096 (2007/10/03)

Routes for the preparation of 2'-silyl protected phosphoramidites of the modified nucleosides O2-methyluridine and O4-methyluridine are described. Methodology for the site-specific incorporation of these phosphonamidetes into a 25 nucleotide long oligoribonucleotide sequence by solid-phase synthesis is reported.

Synthesis of Uridine Analogues to Probe the Functional Group Requirements of the Hairpin Ribozyme

Vyle, Joseph S.,Young, Karen J.,Jones, Sarah,Grasby, Jane A.

, p. S280 - S282 (2007/10/03)

O4-Methyluridine, O2-methyluridine and 4Huridine phosphoramidites were prepared with 2'-O-silyl protection.The methyl modified pyrimidines were synthesised from uridine via the triazolide (O4-methyl) or 2,5'-cyclo derivative (O2-methyl).An improved synthesis of protected 4-thiouridine was also performed.

REACTION OF URACIL NUCLEOSIDES WITH 1-METHYLIMIDAZOLE IN THE PRESENCE OF PHOSPHORYL CHLORIDE: A CONVENIENT METHOD FOR THE SYNTHESIS OF 4-SUBSTITUED PYRIMIDIN-2(1H)-ONE NUCLEOSIDES

Matsuda, Akira,Obi, Kikoh,Miyasaka, Tadashi

, p. 2574 - 2578 (2007/10/02)

Reaction of 2',3',5'-tri-O-benzoyluridine (3) with 1-methylimidazole in the presence of phosphoryl chloride in acetonitrile afforded 3-methyl-1-imidazolium intermediate (4), from which a variety of 4-substituted pyrimidin-2(1H)-one ribosides (5-12) were o

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