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The chemical "5-methyl-1-[4-C-[[[(4-methylphenyl) sulfonyl]oxy]methyl]-3,5-bis-O-(phenylmethyl)-Beta-D-arabinofuranosyl]-2,4(1H,3H)-Pyrimidinedione" is a complex organic compound with a molecular formula of C31H33N3O8S. It features a pyrimidinedione core, which is a type of pyrimidine derivative known for its biological activity. The molecule is characterized by a 5-methyl group attached to the pyrimidinedione ring, and a unique side chain that includes a 4-methylphenyl sulfonyl group connected through an oxymethyl linker to the arabinofuranosyl sugar moiety. This sugar is further modified with two phenylmethyl groups attached to the 3 and 5 positions in a beta configuration. The compound's structure suggests potential applications in medicinal chemistry, possibly as an antiviral or anticancer agent, due to its complex structure and the presence of functional groups that can interact with biological targets.

847666-73-3

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847666-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847666-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,6,6 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 847666-73:
(8*8)+(7*4)+(6*7)+(5*6)+(4*6)+(3*6)+(2*7)+(1*3)=223
223 % 10 = 3
So 847666-73-3 is a valid CAS Registry Number.

847666-73-3SDS

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 2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[4-C-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-3,5-bis-O-(phenylmethyl)-β-D-arabinofuranosyl]-

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

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

More Details:847666-73-3 SDS

847666-73-3Upstream product

847666-73-3Downstream Products

847666-73-3Relevant academic research and scientific papers

Highly stable pyrimidine-motif triplex formation at physiological pH values by a bridged nucleic acid analogue

Rahman, S. M. Abdur,Seki, Sayori,Obika, Satoshi,Haitani, Sunao,Miyashita, Kazuyuki,Imanishi, Takeshi

, p. 4306 - 4309 (2007)

Good things come in threes: A novel bridged nucleic acid in which the furanose conformation was locked in the N form by a six-membered bridged moiety containing an N-O bond (see picture) has been developed. Triplex-forming oligonucleotides composed of thi

Design, synthesis, and properties of 2′,4′-BNANC: A bridged nucleic acid analogue

Rahman, S. M. Abdur,Seki, Sayori,Obika, Satoshi,Yoshikawa, Haruhisa,Miyashita, Kazuyuki,Imanishi, Takeshi

, p. 4886 - 4896 (2008/09/21)

The novel bridged nucleic-acid analogue 2′,4′-BNANC (2′-O,4′-C-aminomethylene bridged nucleic acid), containing a six-membered bridged structure with an N-O linkage, was designed and synthesized efficiently, demonstrating a one-pot intramolecul

NOVEL ARTIFICIAL NUCLEIC ACIDS OF N-O BOND CROSSLINKAGE TYPE

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Page/Page column 15; 18, (2010/11/08)

It is intended to provide oligonucleotide analogs usable in, for exmaple, the antisense method which are highly tolerant to enzymes, have a strong and selective binding affinity for a single-stranded RNA and also are highly capable of forming a triple-str

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