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Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate is a dihydropyrimidine derivative with the molecular formula C10H15NO3S. It is characterized by the presence of an ethyl ester group, a methylthio group, and a carboxylate group. This chemical compound is a yellow, odorless solid with potential pharmacological properties, making it a promising candidate for medicinal chemistry research and drug development.

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  • ETHYL 4-METHYL-2-(METHYLTHIO)-6-OXO-1,6-DIHYDROPYRIMIDINE-5-CARBOXYLATE

    Cas No: 344361-90-6

  • USD $ 1.9-2.9 / Gram

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  • 344361-90-6 Structure
  • Basic information

    1. Product Name: Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate
    2. Synonyms: Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate;ethyl 4-methyl-2-(methylsulfanyl)-6-oxo-1,6-dihydropyrimidine-5-carboxylate
    3. CAS NO:344361-90-6
    4. Molecular Formula: C9H12N2O3S
    5. Molecular Weight: 228.26818
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 344361-90-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 342.1±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.33±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 6.92±0.50(Predicted)
    10. CAS DataBase Reference: Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate(344361-90-6)
    12. EPA Substance Registry System: Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate(344361-90-6)
  • 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: 344361-90-6(Hazardous Substances Data)

344361-90-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate is used as a chemical intermediate in the synthesis of various pharmaceutical compounds. Its unique structural features, including the dihydropyrimidine core, ethyl ester, methylthio, and carboxylate groups, contribute to its potential applications in the development of new drugs with therapeutic benefits.
Used in Medicinal Chemistry Research:
As a dihydropyrimidine derivative, Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate serves as a valuable starting material for medicinal chemistry research. Researchers can modify its structure to explore its potential as a lead compound for the treatment of various diseases and disorders. Its pharmacological properties and chemical reactivity make it an attractive candidate for further investigation and optimization.
Used in Organic Synthesis:
Ethyl 4-Methyl-2-(Methylthio)-6-oxo-1,6-dihydropyriMidine-5-carboxylate can also be employed as an intermediate in organic synthesis for the preparation of other complex organic molecules. Its functional groups, such as the ethyl ester and carboxylate, can be utilized in various synthetic transformations, enabling the synthesis of a wide range of compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 344361-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,3,6 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 344361-90:
(8*3)+(7*4)+(6*4)+(5*3)+(4*6)+(3*1)+(2*9)+(1*0)=136
136 % 10 = 6
So 344361-90-6 is a valid CAS Registry Number.

344361-90-6SDS

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 ethyl 6-methyl-2-methylsulfanyl-4-oxo-1H-pyrimidine-5-carboxylate

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:344361-90-6 SDS

344361-90-6Relevant articles and documents

KINASE INHIBITORS

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Page/Page column 45-46, (2011/05/11)

The present invention provides a new group of protein kinase inhibitors, pyrido[4,3,-d]pyrimidin-5-one derivatives, and pharmaceutically acceptable salts thereof that are useful for intreating cell proliferative disease and disorder such as cancer, autoim

CHEMICAL COMPOUNDS

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Page/Page column 38-39, (2010/04/03)

The invention is directed to pyrido[4,3-d]pyrimidin-5(6H)-one derivatives. Specifically, the invention is directed to compounds according to Formula (I) wherein R1, R2, R3, and R4 are defined below. The compound

METHODS OF TREATING CANCER USING PYRIDOPYRIMIDINONE INHIBITORS OF PI3K ALPHA

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Page/Page column 263-264, (2008/12/04)

The present invention provides methods of treating cancer by administering a compound of Formula I, optionally as a pharmaceutically acceptable salt, solvate and/or hydrate thereof, in combination with other cancer treatments. (Formula I)

PYRIDO [2, 3-D] PYRIMIDIN-7-ONE COMPOUNDS AS INHIBITORS OF PI3K-ALPHA FOR THE TREATMENT OF CANCER

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Page/Page column 74, (2008/12/08)

The invention is directed to a Compound of Formula I, II, or III. The invention provides compounds that inhibit, regulate, and/or modulate PI3K that are useful in the treatment of hyperproliferatives diseases, such as cancer.

PYRIDOPYRIMIDINONE INHIBITORS OF PI3Kα

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Page/Page column 66, (2008/06/13)

The invention is directed to Compounds of Formula I and pharmaceutically acceptable salts or solvates thereof, as well as methods of making and using the compounds.

Solid-phase synthesis of pyrido[2,3-d]pyrimidin-7-ones

Angiolini, Mauro,Bassini, Domenico Fusar,Gude, Markus,Menichincheri, Maria

, p. 8749 - 8752 (2007/10/03)

A novel solid-phase method for the synthesis of 4-methyl-pyrido[2,3-d] pyrimidin-7-one compounds with two diversity points is described. The polymer supported methylsulfonyl derivatives A3, achieved by coupling compound G with different resin-bound amines A1 followed by oxidation with MCPBA, are substituted with several amines R1R2NH. Final cleavage affords 126 compounds having formula H in good yield and purity.

PYRROLYL SUBSTITUTED PYRIDO[2,3-D]PYRIMIDIN-7-ONES AND DERIVATIVES THEREOF AS THERAPEUTIC AGENTS

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Page/Page column 36, (2010/02/14)

The present invention provides pyrimidines of Formula (I): wherein R2, R4, R5, R6, R8 and J have any of the values defined therefor in the specification, and pharmaceutically acceptable salts thereof,

PYRIMIDINES AS INHIBITORS OF PHOSPHOINOSITIDE -3-KINASES (PI3K)

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Page/Page column 45-46, (2008/06/13)

The present invention provides pyrimidines of Formula (I): wherein R4, R6, and Y have any of the values defined therefor in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment

Pyridopyrimidinones derivatives as telomerase inhibitors

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Page/Page column 28-30, (2010/02/05)

The invention provides novel pyrido[2,3-d]pyrimidin-7(8H)-ones derivatives active as telomerase inhibitors, the use of the derivatives as therapeutic agents, such as antitumoral agents, processes for preparation of the derivatives, and to pharmaceutical compositions comprising the derivatives.

Cationic 1,3-diazadienes in annulation reactions. Synthesis of pyrimidine, thiadiazinedioxide and triazine derivatives

Landreau,Deniaud,Reliquet,Reliquet,Meslin

, p. 93 - 98 (2007/10/03)

Triazapentadienium iodides 2 prepared from N'-thiocarbamoylformamidines 1 are efficient intermediates in heterocyclic synthesis. They react with ketenes, sulfenes, phenyl isocyanate or isothiocyanate and dimethyl acetylenedicarboxylate affording the corre

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