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125056-88-4

1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(prop-1-yn-1-yl)pyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125056-88-4 Structure

  • Basic information

    1. Product Name: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(prop-1-yn-1-yl)pyrimidine-2,4(1H,3H)-dione
    2. Synonyms: 1-((2-Hydroxyethoxy)methyl)-6-(2-methylethynyl)thymine; 1-[(2-Hydroxyethoxy)methyl]-6-(2-methylethynyl)thymine; 2,4(1H,3H)-Pyrimidinedione, 1-((2-hydroxyethoxy)methyl)-5-methyl-6-(1-propynyl)-; 2,4(1H,3H)-pyrimidinedione, 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(1-propyn-1-yl)-; 2,4(1H,3H)-Pyrimidinedione, 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(1-propynyl)-
    3. CAS NO:125056-88-4
    4. Molecular Formula: C11H14N2O4
    5. Molecular Weight: 238.2399
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125056-88-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.32g/cm3
    6. Refractive Index: 1.573
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(prop-1-yn-1-yl)pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(prop-1-yn-1-yl)pyrimidine-2,4(1H,3H)-dione(125056-88-4)
    11. EPA Substance Registry System: 1-[(2-hydroxyethoxy)methyl]-5-methyl-6-(prop-1-yn-1-yl)pyrimidine-2,4(1H,3H)-dione(125056-88-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125056-88-4(Hazardous Substances Data)

125056-88-4 Usage

Molecular structure

The compound has a complex molecular structure with a pyrimidine ring as its core.

Pyrimidine ring

The core of the molecule is a pyrimidine ring, which is a six-membered heterocyclic aromatic ring with four carbon atoms and two nitrogen atoms.

Hydroxyethoxy methyl group

The compound contains a hydroxyethoxy methyl group attached to the pyrimidine ring. This group consists of an ethoxy (-OCH2CH2-) chain with a hydroxyl (-OH) group at one end.

Methyl group

A methyl (-CH3) group is also attached to the pyrimidine ring, providing additional steric bulk and potential sites for interaction with other molecules.

Propynyl group

The compound features a propynyl (prop-1-yn-1-yl) group, which is a three-carbon chain with a triple bond at one end and a hydrogen atom at the other. This group adds further complexity to the molecule and may influence its reactivity and biological activity.

Pyrimidine-2,4-dione derivative

The compound is a derivative of pyrimidine-2,4-dione, which means it has two carbonyl (C=O) groups at the 2nd and 4th positions of the pyrimidine ring.

Potential biological activity

Due to its unique structure, the compound may exhibit biological activity, making it a candidate for further research in pharmaceuticals, agriculture, or materials science.

Applications

The compound may have potential applications in various fields, including drug development, agrochemicals, and the creation of new materials with specific properties.

Further research and development

To fully understand the properties and potential uses of this chemical compound, additional research and development may be necessary.

Check Digit Verification of cas no

The CAS Registry Mumber 125056-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,5 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125056-88:
(8*1)+(7*2)+(6*5)+(5*0)+(4*5)+(3*6)+(2*8)+(1*8)=114
114 % 10 = 4
So 125056-88-4 is a valid CAS Registry Number.

125056-88-4Relevant articles and documents

6-substituted acyclopyrimidine nucleoside derivatives and antiviral agents containing the same as active ingredient thereof

-

, (2008/06/13)

6-substitutted acyclopyrimidine nucleoside derivatives represented by the following general formula I: STR1 wherein R1 represents a hydrogen or halogen atom or a group of alkyl, alkenyl, alkynyl, alkylcarbonyl, arylcarbonyl, arylcarbonylalkyl,

A new class of HIV-1-specific 6-substituted acyclouridine derivatives: Synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)

Tanaka,Baba,Hayakawa,Sakamaki,Miyasaka,Ubasawa,Takashima,Sekiya,Nitta,Shigeta,Walker,Balzarini,De Clercq

, p. 349 - 357 (2007/10/02)

A series of novel acyclouridine derivatives substituted at both the C-5 and C-6 positions were synthesized for the purpose of improving the activity of a recently reported HIV-1-specific lead, 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT). Prep

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