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Uridine 6-methyl 2',3',5'-tribenzoate is a chemical compound derived from the nucleoside uridine, which is a component of RNA. In this specific compound, the uridine molecule is modified by the addition of three benzoate groups at the 2', 3', and 5' positions of the ribose sugar moiety, and a methyl group is attached to the 6th position of the uracil base. This modification can affect the compound's properties, such as solubility, stability, and interaction with enzymes or other biomolecules. The compound may be used in various applications, including research and development in the fields of molecular biology, drug design, and chemical synthesis.

23316-76-9

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23316-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23316-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,1 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23316-76:
(7*2)+(6*3)+(5*3)+(4*1)+(3*6)+(2*7)+(1*6)=89
89 % 10 = 9
So 23316-76-9 is a valid CAS Registry Number.

23316-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',3',5'-tri-O-benzoyl-6-methyluridine

1.2 Other means of identification

Product number -
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

1.5 Emergency phone number

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More Details:23316-76-9 SDS

23316-76-9Relevant academic research and scientific papers

Stereoselective synthesis of N1-6-methyluridine and related 2-substituted analogues

Radi, Marco,Petricci, Elena,Corelli, Federico,Botta, Maurizio

, p. 79 - 83 (2008/02/13)

Coupling reaction of 2-substituted-6-methyl-4(3H)-pyrimidinones (1a,b) with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose (ABR) afforded the corresponding N1-2,6-disubstituted nucleosides (2a,b) without any trace of the N3-isomer.

Nucleoside Syntheses, XXII. Nucleoside Synthesis with Trimethylsilyl Triflate and Perchlorate as Catalysts

Vorbrueggen, Helmut,Krolikiewicz, Konrad,Bennua, Baerbel

, p. 1234 - 1255 (2007/10/02)

The novel Lewis acids (CH3)3SiOSO2CF3 (5), (CH3)3SiOSO2C4F9 (6), and (CH3)3SiClO4 (4) are highly selective and efficient Friedel-Crafts catalysts for nucleoside formation from silylated heterocycles and peracylated sugars as well as for rearrangements of persilylated protected nucleosides.With basic silylated heterocycles these new catalysts give much higher yields of the natural N-1-nucleosides than with SnCl4.

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