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165807-06-7

4-Pyrimidinecarboxaldehyde, 2-amino(9CI), also known by its CAS Registry Number 69849-43-6, is a chemical compound that belongs to the class of organic compounds known as pyrimidines and pyrimidine derivatives. These are aromatic heterocyclic compounds characterized by a pyrimidine ring, which is a six-membered ring with two nitrogen atoms and four carbon atoms. Although the exact structure, properties, and potential applications of this compound are not extensively documented in literature, it can be inferred that it may have potential uses in various industries due to its classification.

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  • 165807-06-7 Structure

  • Basic information

    1. Product Name: 4-Pyrimidinecarboxaldehyde, 2-amino- (9CI)
    2. Synonyms: 4-Pyrimidinecarboxaldehyde, 2-amino- (9CI);2-Amino-4-pyrimidinecarboxaldehyde;2-aMinopyriMidine-4-carbaldehyde
    3. CAS NO:165807-06-7
    4. Molecular Formula: C5H5N3O
    5. Molecular Weight: 123.1127
    6. EINECS: N/A
    7. Product Categories: PYRIMIDINE;pharmacetical
    8. Mol File: 165807-06-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 372.7 °C at 760 mmHg
    3. Flash Point: 179.2 °C
    4. Appearance: /
    5. Density: 1.37 g/cm3
    6. Vapor Pressure: 9.47E-06mmHg at 25°C
    7. Refractive Index: 1.666
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 2.03±0.10(Predicted)
    11. CAS DataBase Reference: 4-Pyrimidinecarboxaldehyde, 2-amino- (9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Pyrimidinecarboxaldehyde, 2-amino- (9CI)(165807-06-7)
    13. EPA Substance Registry System: 4-Pyrimidinecarboxaldehyde, 2-amino- (9CI)(165807-06-7)

  • 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: 165807-06-7(Hazardous Substances Data)

165807-06-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Pyrimidinecarboxaldehyde, 2-amino(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, containing both a pyrimidine ring and an aldehyde group, makes it a valuable building block for the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agricultural Industry:
In the agricultural industry, 4-Pyrimidinecarboxaldehyde, 2-amino(9CI) may be used as a precursor for the development of novel agrochemicals, such as pesticides or herbicides. Its potential activity against pests or weeds could be explored, and its incorporation into these products could lead to more effective and targeted agricultural solutions.
Used in Scientific Research:
4-Pyrimidinecarboxaldehyde, 2-amino(9CI) is used as a research compound in various scientific studies. Its unique structure and potential reactivity make it an interesting subject for investigation in the fields of organic chemistry, biochemistry, and materials science. Researchers may explore its potential interactions with biological molecules, its use in the synthesis of new compounds, or its application in the development of new materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 165807-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,0 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 165807-06:
(8*1)+(7*6)+(6*5)+(5*8)+(4*0)+(3*7)+(2*0)+(1*6)=147
147 % 10 = 7
So 165807-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N3O/c6-5-7-2-1-4(3-9)8-5/h1-3H,(H2,6,7,8)

165807-06-7SDS

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-aminopyrimidine-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Aminopyrimidine-4-carboxaldehyde

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:165807-06-7 SDS

165807-06-7Relevant articles and documents

NEW THIENOPYRIMIDINE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Page/Page column 141; 142, (2015/07/15)

Compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, R12, X, A and n are as defined in the description.

8-SUBSTITUTED 2-(BENZIMIDAZOLYL)PURINE DERIVATIVES FOR IMMUNOSUPPRESSION

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Page/Page column 17, (2008/06/13)

The present invention provides novel purines useful for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection. The compounds are of the general formula I:

8-HETEROARYLPURINE MNK2 INHIBITORS FOR TREATING METABOLIC DISORDERS

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Page/Page column 37, (2010/11/28)

This invention relates to 8-Heteroarylpurine Mnk2 Inhibitors which are useful for the treatment and prevention of metabolic disorders such as obesity and diabetes.

Isonitrile intermediates for the preparation of tri-substituted imidazole compounds with multiple therapeutic properties

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Page 25, (2010/01/31)

The invention relates to a novel group of isonitrile compounds and a process for their preparation, useful in the preparation of tri-substituted imadazoles having multiple therapeutic properties.

Pyrimidinylimidazole inhibitors of CSBP/P38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes

Adams, Jerry L.,Boehm, Jeffrey C.,Kassis, Shouki,Gorycki, Peter D.,Webb, Edward F.,Hall, Ralph,Sorenson, Margaret,Lee, John C.,Ayrton, Andrew,Griswold, Don E.,Gallagher, Timothy F.

, p. 3111 - 3116 (2007/10/03)

Pyrimidine analogs of the pyridinylimidazole class of CSBP/p38 kinase inhibitors were prepared in an effort to reduce the potent inhibition of hepatic cytochrome P450 observed for the pyridinyl compounds. The substitution of pyrimidin-4-yl, 2-methoxypyrimidin-4-yl, or 2- methylaminopyrimidin-4-yl for pyridin-4-yl effectively dissociates CSBP/p38 kinase from P450 inhibition for this series and furthermore achieves an increase in oral activity.

Imidazole compounds, use and process of making

-

, (2008/06/13)

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

Pyridyl imidazole compounds and compositions

-

, (2008/06/13)

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

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