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CAS

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96548-91-3

4-Pyrimidinamine, 2-fluoro(9CI) is a chemical compound with the molecular formula C4H3FN4. It is a derivative of pyrimidine with a fluorine atom attached at the 2 position. 4-Pyrimidinamine, 2-fluoro(9CI) is of interest to researchers due to its potential applications in various fields, particularly in the pharmaceutical and agrochemical industries.

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  • 96548-91-3 Structure

  • Basic information

    1. Product Name: 4-Pyrimidinamine, 2-fluoro- (9CI)
    2. Synonyms: 4-Pyrimidinamine, 2-fluoro- (9CI);2-fluoropyrimidin-4-amine
    3. CAS NO:96548-91-3
    4. Molecular Formula: C4H4FN3
    5. Molecular Weight: 113.0930632
    6. EINECS: N/A
    7. Product Categories: PYRIMIDINE
    8. Mol File: 96548-91-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 324.9±34.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.372±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. PKA: 2.58±0.10(Predicted)
    10. CAS DataBase Reference: 4-Pyrimidinamine, 2-fluoro- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Pyrimidinamine, 2-fluoro- (9CI)(96548-91-3)
    12. EPA Substance Registry System: 4-Pyrimidinamine, 2-fluoro- (9CI)(96548-91-3)

  • 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: 96548-91-3(Hazardous Substances Data)

96548-91-3 Usage

Uses

Used in Pharmaceutical Industry:
4-Pyrimidinamine, 2-fluoro(9CI) is used as a building block for the synthesis of various biologically active molecules. Its unique structure and fluorinated nature contribute to the development of new drugs with improved properties, such as enhanced bioavailability, selectivity, and potency.
Used in Agrochemical Industry:
In the agrochemical field, 4-Pyrimidinamine, 2-fluoro(9CI) serves as a key intermediate in the synthesis of agrochemicals with potential pesticidal or herbicidal activities. Its incorporation into these molecules can lead to the development of more effective and environmentally friendly products.
Used in Fluorine Chemistry Research:
4-Pyrimidinamine, 2-fluoro(9CI) is also used as a valuable tool in the study of fluorine chemistry. Its presence in various molecular structures allows researchers to explore the effects of fluorination on the properties and reactivity of compounds, which can be crucial in drug design and development.

Check Digit Verification of cas no

The CAS Registry Mumber 96548-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,4 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96548-91:
(7*9)+(6*6)+(5*5)+(4*4)+(3*8)+(2*9)+(1*1)=183
183 % 10 = 3
So 96548-91-3 is a valid CAS Registry Number.

96548-91-3SDS

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-fluoropyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 2-fluoro-pyrimidin-4-ylamine

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:96548-91-3 SDS

96548-91-3Upstream product

96548-91-3Relevant articles and documents

Peptide deformylase inhibitors

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Page/Page column, (2014/12/09)

The present invention relates to a compound of Formula (I): or a pharmaceutically acceptable salt thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods directed to bacterial infections and inhibition of bacterial peptide deformylase (PDF) activity.

PEPTIDE DEFORMYLASE INHIBITORS

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Page/Page column, (2014/02/15)

The present invention relates to a compound of Formula (I): or a pharmaceutically acceptable salt thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods directed to bacterial infections and inhi-bition of bacterial peptide deformylase (PDF) activity

SUBSTITUTED HETEROCYCLIC COMPOUNDS AND METHODS OF USE

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Page/Page column 43, (2010/10/20)

The present invention relates to pyridines, pyrimidines and derivatives thereof, and pharmaceutically acceptable salts thereof. Also included is a method of treatment of inflammation, rheumatoid arthritis, Pagets disease, osteoporosis, multiple myeloma, uveititis, acute or chronic myelogenous leukemia, pancreatic beta cell destruction, osteoarthritis, rheumatoid spondylitis, gouty arthritis, inflammatory bowel disease, adult respiratory distress syndrome (ARDS), psoriasis, Crohn's disease, allergic rhinitis, ulcerative colitis, anaphylaxis, contact dermatitis, asthma, muscle degeneration, cachexia, Reiter's syndrome, type I diabetes, type II diabetes, bone resorption diseases, graft vs. host reaction, Alzheimer's disease, stroke, myocardial infarction, ischemia reperfusion injury, atherosclerosis, brain trauma, multiple sclerosis, cerebral malaria, sepsis, septic shock, toxic shock syndrome, fever, myalgias due to HIV-1, HIV-2, HIV-3, cytomegalovirus (CMV), influenza, adenovirus, the herpes viruses or herpes zoster infection in a mammal comprising administering an effective amount a compound as described above.

Fluorinated Heterocyclic Compounds. 2. 2,4-Difluoro and 4-Amino-2-fluoropyrimidines, Nucleoside Base Analogs

Svirskaya, Polina I.,Yedidia, Varda,Leznoff, Clifford C.,Miller, Jack M.

, p. 149 - 153 (2007/10/02)

Nucleoside base analogs in which fluoro substituents replace the enolic hydroxy groups of uracil, thymine and cytosine have been prepared.Improved methods for the preparation and isolation of the known 2,4-difluoropyrimidine, 2,4-difluoro-6-methylpyrimidine and the new 2,4-difluoro-5-methylpyrimidine, 2-fluoro-4-aminopyrimidine, 4-fluoro-2-aminopyrimidine, and other alkylaminofluoropyrimidines are described.

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