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CAS

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164738-44-7

4-Pyrimidinecarboxaldehyde, 2-methoxy(9CI) is an organic compound with the molecular formula C6H5NO2. It is a derivative of pyrimidine, a heterocyclic compound with potential applications in various fields due to its unique chemical properties.

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  • 164738-44-7 Structure

  • Basic information

    1. Product Name: 4-Pyrimidinecarboxaldehyde, 2-methoxy- (9CI)
    2. Synonyms: 4-Pyrimidinecarboxaldehyde, 2-methoxy- (9CI);2-Methoxy-4-pyriMidinecarbaldehyde
    3. CAS NO:164738-44-7
    4. Molecular Formula: C6H6N2O2
    5. Molecular Weight: 138.12404
    6. EINECS: 205-525-8
    7. Product Categories: PYRIMIDINE;Heterocycle-Pyrimidine series
    8. Mol File: 164738-44-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 281.3°C at 760 mmHg
    3. Flash Point: 123.9°C
    4. Appearance: /
    5. Density: 1.238g/cm3
    6. Vapor Pressure: 0.0036mmHg at 25°C
    7. Refractive Index: 1.556
    8. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    9. Solubility: N/A
    10. PKA: -0.53±0.23(Predicted)
    11. CAS DataBase Reference: 4-Pyrimidinecarboxaldehyde, 2-methoxy- (9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Pyrimidinecarboxaldehyde, 2-methoxy- (9CI)(164738-44-7)
    13. EPA Substance Registry System: 4-Pyrimidinecarboxaldehyde, 2-methoxy- (9CI)(164738-44-7)

  • 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: 164738-44-7(Hazardous Substances Data)

164738-44-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Pyrimidinecarboxaldehyde, 2-methoxy(9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to form a wide range of derivatives makes it a valuable building block in the development of new drugs.
Used in Antiviral Applications:
In the field of antiviral research, 4-Pyrimidinecarboxaldehyde, 2-methoxy(9CI) is used as a precursor in the preparation of piperidine derivatives. These derivatives have been identified as inhibitors of the Hepatitis C Virus (HCV) polymerase, an essential enzyme for the replication of the virus. By inhibiting the polymerase, these compounds can potentially slow down or stop the replication of HCV, making them promising candidates for the development of antiviral drugs against Hepatitis C.

Check Digit Verification of cas no

The CAS Registry Mumber 164738-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,3 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 164738-44:
(8*1)+(7*6)+(6*4)+(5*7)+(4*3)+(3*8)+(2*4)+(1*4)=157
157 % 10 = 7
So 164738-44-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-10-6-7-3-2-5(4-9)8-6/h2-4H,1H3

164738-44-7SDS

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-Methoxypyrimidine-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-pyrimidinecarbaldehyde,2-methoxy

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:164738-44-7 SDS

164738-44-7Relevant articles and documents

Cycloalkyl substituted imidazoles

-

, (2008/06/13)

Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy.

Substituted imidazole compounds

-

, (2008/06/13)

Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.

Diazines. 13. Metalation without Ortho-Directing Group Functionalization of Diazines via Direct Metalation

Ple, Nelly,Turck, Alain,Couture, Karine,Queguiner, Guy

, p. 3781 - 3786 (2007/10/02)

The successful metalation of diazines without an ortho-directing group is described.In some cases, dimers were obtained.The metalation was optimal with LTMP if a 4-fold excess of metalating agent was used, with a very short metalation reaction time at -75

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