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2-Ethylthio-5-methyl-3H-pyrimidin-4-one, also known as 2-ethylthio-5-methyluracil, is a pyrimidinone derivative featuring an ethylthio group and a methyl group attached to the pyrimidine ring. This chemical compound holds potential pharmaceutical applications and has been studied for its antiviral and antitumor activities, making it a promising candidate for treating specific medical conditions. Additionally, it serves as a valuable biochemical tool in research settings for a range of experimental purposes.

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  • 13480-95-0 Structure
  • Basic information

    1. Product Name: 2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE
    2. Synonyms: 2-ETHYLTHIO-4-HYDROXY-5-METHYLPYRIMIDINE;2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE;RARECHEM AH CK 0102;2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE 98%;2-Ethylthio-4-hydroxy-5-methylpyrimidine 98%;4(1H)-Pyrimidinone, 2-(ethylthio)-5-methyl-;2-(Ethylthio)-5-methyl-4(1H)-pyrimidinone;2-(Ethylthio)-5-methylpyrimidine-4(1H)-one
    3. CAS NO:13480-95-0
    4. Molecular Formula: C7H10N2OS
    5. Molecular Weight: 170.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13480-95-0.mol
  • Chemical Properties

    1. Melting Point: 185 °C
    2. Boiling Point: 274.4 °C at 760 mmHg
    3. Flash Point: 119.8 °C
    4. Appearance: /
    5. Density: 1.25 g/cm3
    6. Vapor Pressure: 0.00542mmHg at 25°C
    7. Refractive Index: 1.601
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 8.06±0.50(Predicted)
    11. CAS DataBase Reference: 2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE(13480-95-0)
    13. EPA Substance Registry System: 2-ETHYLTHIO-5-METHYL-3H-PYRIMIDIN-4-ONE(13480-95-0)
  • Safety Data

    1. Hazard Codes: Xi
    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: 13480-95-0(Hazardous Substances Data)

13480-95-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Ethylthio-5-methyl-3H-pyrimidin-4-one is used as a drug candidate for its potential antiviral and antitumor activities, targeting the development of treatments for certain medical conditions.
Used in Research Laboratories:
In the scientific community, 2-ethylthio-5-methyl-3H-pyrimidin-4-one is utilized as a biochemical tool, facilitating various experimental procedures and contributing to the advancement of knowledge in related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 13480-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13480-95:
(7*1)+(6*3)+(5*4)+(4*8)+(3*0)+(2*9)+(1*5)=100
100 % 10 = 0
So 13480-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2OS/c1-3-11-7-8-4-5(2)6(10)9-7/h4H,3H2,1-2H3,(H,8,9,10)

13480-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanyl-5-methyl-1H-pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names MPXDEUQRWKVZBD-UHFFFAOYSA

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:13480-95-0 SDS

13480-95-0Relevant articles and documents

Reactions with 2-thiothymine; selective cyclization of S-substituted 2-thiothymine

Youssef, Mohamed M.,Youssef, Ayman M. S.

, p. 67 - 81 (2007/10/03)

2-Thiothymine (I) undergoes S-alkylation when treated with some halo compounds such as methyl and ethyl iodides. The S-alkyl derivatives II are treated with hydrazine hydrate to produce the hydrazine derivative III, which condensed with p-chlorobenzaldehyde to give p-chlorobenzaldehydepyrimidinehydrazone derivative IV. Compound IIa reacts with phosphorus oxychloride to give 4-chloro derivative V. The chlorine atom in V undergoes nucleophilic substitution with p-chloroaniline and anthranilic acid to produce drivatives VIa,b. Dehydrative cyclization of VIb yields the pyrimido[6,1-b]quinazolin-10-one derivative VII. Treatment of V with ammonia solution gives the diamino derivative VId. Reaction of V with sodium azide produces the tetrazolo[1,5-c]pyrimidine derivative VIII. Compound I undergoes S-alkylation with α-haloketones followed by cyclization to produce the thiazolo[3,2-a]pyrimidine derivatives Xa-c. Reaction of I with bromomalononitrile produces thiazolo[3,2-a]pyrimidine-2-carbonitrile derivative XII. Treatment of XII with formic acid, formamide and ammonium thiocyanate produces thiazolo[3,2-a:4,5-d]dipyrimidine derivatives XIIIa-c. Finally, reacting XII with malononitrile yields ppyrido[2′,3′:4,5]thiazolo[3,2-a]pyrimidine-3-carbonitrile derivative XIV.

Src kinase inhibitor compounds

-

, (2008/06/13)

Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.

Synthesis of S2-alkyl-2-thiouridines

Abdel-Rahman, Adel A.-H.,Zahran, Magdy A.,Abdel-Megied, Ahmed E.-S.,Pedersen, Erik B.,Nielsen, Claus

, p. 237 - 241 (2007/10/03)

5-Substituted S2-alkyl-2-thiouracils 1a-i were treated with 1,1,1,3,3,3-hexamethyldisilazane and ammonium sulfate at reflux temperature and condensed with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose in acetonitrile using trimethylsilyl trifluoromet

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