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145414-66-0

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145414-66-0 Usage

Molecular structure

The compound has a complex molecular structure, consisting of a pyrimidine ring with a methyl group and a dioxolane ring with a hydroxymethyl group.

Stereochemistry

The compound has specific stereochemistry, with the 2S,4R configuration at the dioxolane ring.

Functional groups

The compound contains a hydroxymethyl group, a methyl group, and two carbonyl groups (one at each position 2 and 4 of the pyrimidine ring).

Potential applications

The compound is a potential antiviral agent and has been studied for its potential use in the treatment of cancer.

Pharmaceutical research

Due to its unique molecular structure and potential therapeutic properties, the compound may have applications in pharmaceutical research and drug development.

Molecular weight

The molecular weight of the compound is approximately 236.21 g/mol.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, etc.) is not provided in the material, but it may be influenced by the presence of the dioxolane ring and the carbonyl groups.

Synthesis

The synthesis of the compound is not described in the material, but it likely involves the formation of the pyrimidine ring, the dioxolane ring, and the attachment of the hydroxymethyl and methyl groups.

Check Digit Verification of cas no

The CAS Registry Mumber 145414-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,4,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145414-66:
(8*1)+(7*4)+(6*5)+(5*4)+(4*1)+(3*4)+(2*6)+(1*6)=120
120 % 10 = 0
So 145414-66-0 is a valid CAS Registry Number.

145414-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2S,4R)-2-(hydroxymethyl)-1,3-dioxolan-4-yl]-5-methylpyrimidine-2,4-dione

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:145414-66-0 SDS

145414-66-0Downstream Products

145414-66-0Relevant articles and documents

2-Substituted-4-substituted-1,3-dioxolanes and use thereof

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Page column 51 -52, (2010/11/29)

Nucleoside analogues containing a 1,3-dioxolane structure are suitable antiviral agents, particulary for the treatment of the HIV infections in mammals, especially humans. Examples of the nucleoside analogues include: cis-2-acetoxymethyl-4-(thymin-1′-yl)-1,3,-dioxolane, cis-2-hydroxymethyl-4-(thymin-1′-yl)-1,3-dioxolane, cis-2-benzoyloxymethyl-4-(cytosin-1′-yl)-1,3-dioxolane, and cis-2-hydroxymethyl-4-(cytosin-1′-yl)-1,3-dioxolane. These compounds can be in the form of their racemates or their separate enantiomers.

In situ complexation directs the stereochemistry of N-glycosylation in the synthesis of oxathiolanyl and dioxolanyl nucleoside analogues

Choi, Woo-Baeg,Wilson, Lawrence J.,Yeola, Suresh,Liotta, Dennis C.,Schinazi, Raymond F.

, p. 9377 - 9379 (2007/10/02)

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