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Uridine 3-benzoyl 2',3',5'-triacetate is a complex organic compound with the molecular formula C21H23N2O9. It is a derivative of uridine, a nucleoside composed of uracil and ribose, where the 3-position of uridine is modified with a benzoyl group, and the 2', 3', and 5' positions of the ribose are acetylated. This chemical is often used in biochemical research, particularly in studies involving RNA synthesis and modification, as well as in the development of antiviral drugs. Its unique structure allows it to interact with various enzymes and proteins, making it a valuable tool for understanding the mechanisms of RNA processing and for designing new therapeutic agents.

31077-36-8

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31077-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31077-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,7 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31077-36:
(7*3)+(6*1)+(5*0)+(4*7)+(3*7)+(2*3)+(1*6)=88
88 % 10 = 8
So 31077-36-8 is a valid CAS Registry Number.

31077-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name O2',O3',O5'-triacetyl-3-benzoyl-uridine

1.2 Other means of identification

Product number -
Other names Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(3-benzoyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31077-36-8 SDS

31077-36-8Downstream Products

31077-36-8Relevant academic research and scientific papers

Transprotection of N-benzoylated nucleobase derivatives by dialkylaminomethylene group

Endova, Magdalena,Masojidkova, Milena,Rosenberg, Ivan

, p. 2151 - 2164 (2007/10/03)

The use of (chloromethylene)dialkylammonium chloride in selective transprotection of N-benzoylated nucleobase derivatives is reported along with the evaluation of the stability of various protecting groups widely used in nucleoside and/or nucleotide chemi

AN EFFECTIVE METHOD FOR THE PREPARATION OF O6-SUBSTITUTED GUANOSINE AND N3-SUBSTITUTED URIDINE DERIVATIVES VIA THE CORRESPONDING STANNYLATED INTERMEDIATES

Tanimura, Hiroshi,Sekine, Mitsuo,Hata, Tsujiaki

, p. 4047 - 4050 (2007/10/02)

O6-substituted guanosine and N3-substituted uridine derivatives were obtained in high yields by stannylation of the corresponding unsubstituted nucleosides with bis(tributyltin)-oxide followed by treatment with various electrophiles.

Structural assignment of n3-acylated uridine derivatives by means of 13C NMR spectroscopy

Kamimura,Masegi,Sekine,Hata

, p. 4241 - 4244 (2007/10/02)

Diisopropylethylamine was effective as a base for acylation of 2',3',5'-tri-O-acetyluridine with various acid chlorides. The 13C NMR spectra of the products and related compounds showed clearly that the acyl groups introduced to the uracil moie

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