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1-[(1R,3S,4R)-3-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-methylpyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61849-27-2

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61849-27-2 Usage

Molecular structure

The compound has a complex molecular structure consisting of a cyclopentyl ring with a hydroxymethyl and hydroxyl group attached, as well as a pyrimidine ring with a methyl substituent.

Stereochemistry

The compound has specific stereochemistry, with the hydroxyl group at the 3-position and the hydroxymethyl group at the 4-position of the cyclopentyl ring, and the methyl group at the 5-position of the pyrimidine ring.

Potential pharmaceutical properties

The compound may have potential pharmaceutical properties due to its unique structure and potential biological activities.

Drug development interest

The compound may be of interest for drug development, as further study is needed to fully understand its properties and potential uses.

Further study needed

Further research is required to fully understand the properties and potential uses of 1-[(1R,3S,4R)-3-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-methylpyrimidine-2,4(1H,3H)-dione, including its pharmacological activity, safety, and efficacy.

Molecular weight

The molecular weight of the compound is approximately 222.24 g/mol.

Solubility

The solubility of the compound in various solvents is not provided in the material, but it may be influenced by its polar and nonpolar functional groups.

Stability

The stability of the compound under different conditions, such as temperature, pH, and light exposure, is not provided in the material and would need to be determined through further study.

Synthesis

The synthesis of the compound is not described in the material, but it likely involves the formation of the cyclopentyl and pyrimidine rings, as well as the introduction of the hydroxymethyl, hydroxyl, and methyl substituents.

Check Digit Verification of cas no

The CAS Registry Mumber 61849-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,4 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61849-27:
(7*6)+(6*1)+(5*8)+(4*4)+(3*9)+(2*2)+(1*7)=142
142 % 10 = 2
So 61849-27-2 is a valid CAS Registry Number.

61849-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4(1H,3H)-Pyrimidinedione, 1-[3-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-methyl-, (1.α.,3.β.,4.α.)-(+-)-

1.2 Other means of identification

Product number -
Other names Camphor,d-oxime

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:61849-27-2 SDS

61849-27-2Relevant academic research and scientific papers

New and efficient synthesis of racemic cyclopent-3-en-1-yl nucleoside analogues and their derivatives

Reichardt, Bastian,Ludek, Olaf R.,Meier, Chris

, p. 1011 - 1028 (2008/02/07)

A new, efficient synthesis of racemic cyclopent-3-en-1-yl nucleoside analogues has been developed starting from cyclopentadiene. The key step is the regioselective hydroboration of an intermediately formed mixture of two alkylated cyclopentadienes to give

2-azabicyclo[2.2.1]hept-5-en-3-one epoxide: A versatile intermediate for the synthesis of cyclopentyl carbocyclic 2-deoxy-, 3-deoxy- and ara- ribonucleoside analogues.

Dominguez, Belen M.,Cullis, Paul M.

, p. 5783 - 5786 (2007/10/03)

5,6-Epoxy-exo-2-azabicyclo[2.2.1]heptan-3-one has been used as a versatile intermediate in the synthesis of 2-deoxy-, 3-deoxy- and ara- cyclopentyl carbocyclic nucleosides. An efficient, short synthesis of the (+) carbocyclic thymidine 13 is reported.

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