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6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone is a pyrimidinone class chemical compound, a derivative of pyrimidine, featuring a hydroxy, methoxy, and methyl group. It has been studied for its potential biological and pharmacological activities, such as antioxidant, anti-inflammatory, and anticancer properties. This unique structure and its properties make it a promising target for further research and development, with potential applications in pharmaceutical drug development and organic synthesis.

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  • 851985-99-4 Structure
  • Basic information

    1. Product Name: 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone
    2. Synonyms: 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone;6-Hydroxy-5-methoxy-2-methylpyrimidin-4(3H)-one
    3. CAS NO:851985-99-4
    4. Molecular Formula: C6H8N2O3
    5. Molecular Weight: 156.13932
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851985-99-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.42±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 5.66±0.10(Predicted)
    10. CAS DataBase Reference: 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone(851985-99-4)
    12. EPA Substance Registry System: 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone(851985-99-4)
  • 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: 851985-99-4(Hazardous Substances Data)

851985-99-4 Usage

Uses

Used in Pharmaceutical Development:
6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone is used as a pharmaceutical candidate for its potential antioxidant, anti-inflammatory, and anticancer properties. Its unique structure allows it to be a promising target for the development of new drugs that can address various health conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 6-hydroxy-5-methoxy-2-methyl-4(3H)-Pyrimidinone is used as a key intermediate or building block for the synthesis of more complex organic compounds. Its versatile functional groups enable it to be a valuable component in the creation of novel molecules with specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 851985-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,8 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 851985-99:
(8*8)+(7*5)+(6*1)+(5*9)+(4*8)+(3*5)+(2*9)+(1*9)=224
224 % 10 = 4
So 851985-99-4 is a valid CAS Registry Number.

851985-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4,6-dihydroxy-5-methoxy-pyrimidine

1.2 Other means of identification

Product number -
Other names 5-methoxy-2-methylpyrimidine-4,6-diol

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:851985-99-4 SDS

851985-99-4Downstream Products

851985-99-4Relevant articles and documents

Pyrimidine Derivatives Which Are Antagonists Of Vitronectin Receptor

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Page/Page column 20, (2010/11/30)

A subject of the invention is the compounds of formula (I); in which R1, R2, R3, R4 and R have the meanings indicated in the description, their preparation process, their use as medicaments having an antagonist activity on the vitronectin receptor and the pharmaceutical compositions containing them.

SUBSTITUTED NITROGEN-CONTAINING SIX-MEMBERED AMINO-HETEROCYCLES AS VANILLOID-1 RECEPTOR ANTAGONISTS FOR TREATING PAIN

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Page/Page column 40, (2010/02/11)

The present invention provides a compound of formula (I): Y-J-NH-Z wherein: Y is a quinoline or isoquinoline optionally substituted with one or two substituents independently chosen from hydroxy, halogen, haloC1-4alkyl, C1-4alkyl, C1-4alkoxy, haloC1-4alkoxy, nitro and amino; J is pyridine, pyridazine, pyrazine, pyrimidine or triazine optionally substituted with one or two substituents independently chosen from hydroxy, halogen, haloC1-4alkyl, C1-4alkyl, C3-5cycloalkyl, C1-4alkoxy, hydroxyC1-4alkyl, cyano, hydroxy, C1-4cycloalkoxy, C1-4alkylthio, haloC1-4alkoxy, nitro, Q, (CH2)pQ, NR2R3, -(CH2)pNR2R3 and -O(CH2)pNR2R3; wherein J is substituted at positions meta to each other by NH and Y; and Z is phenyl or pyridyl optionally substituted with one or two substituents independently selected from halogen, haloC1-4alkyl, C1-4alkyl, C1-4alkoxy, haloC1-4alkoxy, nitro and amino; Q is phenyl, a five-membered heterocyclic ring containing one, two, three or four heteroatoms chosen from O, N and S, at most one heteroatom being O or S, or a six-membered heterocyclic ring containing one, two or three nitrogen atoms, optionally substituted by C1-4alkyl; each R2 and R3 is chosen from H and C1-4alkyl, or R2 and R3, together with the nitrogen atom to which they are attached, may form a six-membered ring optionally containing an oxygen atom or a further nitrogen atom, which ring is optionally substituted by C1-4alkyl or Q; p is 1, 2 or 3; or a pharmaceutically acceptable salt thereof; pharmaceutical compositions comprising it; its use in methods of therapy; use of it for manufacturing medicaments; and methods of using it to treat diseases requiring administration of a VR1 antagonist such as pain, cough, GERD and depression.

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