(1,3-dimethyl-1H-pyrazol-4-yl)methanamine

Base Information

• Chemical Name: (1,3-dimethyl-1H-pyrazol-4-yl)methanamine
• CAS No.: 400756-28-7
• Molecular Formula: C6H11N3
• Molecular Weight: 125.17164
• Hs Code.: 2933199090
• DSSTox Substance ID: DTXSID70361397
• Wikidata: Q72471810
• Mol file: 400756-28-7.mol

Synonyms:(1,3-dimethyl-1H-pyrazol-4-yl)methanamine;400756-28-7;(1,3-dimethyl-1H-pyrazol-4-yl)methylamine;(1,3-dimethylpyrazol-4-yl)methanamine;C-(1,3-Dimethyl-1H-pyrazol-4-yl)-methylamine;MFCD02055709;C-(1,3-Dimethyl-1H-pyrazol-4-yl)methylamine;1-(1,3-dimethyl-1H-pyrazol-4-yl)methanamine;1H-Pyrazole-4-methanamine, 1,3-dimethyl-;SCHEMBL261837;DTXSID70361397;1,3-Dimethylpyrazole-4-methanamine;AMY32862;STK288938;AKOS000304236;AB10627;GS-6094;SY081005;BB 0259472;CS-0054471;FT-0678895;A26132;EN300-129823;H10414;(1,3-Dimethyl-1H-pyrazol-4-yl)methylamine, AldrichCPR;C-(1,3-DIMETHYL-1H-PYRAZOL-4-YL)-METHANAMINE;F2169-0316

Chemical Property of (1,3-dimethyl-1H-pyrazol-4-yl)methanamine

Chemical Property:

• Vapor Pressure: 0.0567mmHg at 25°C
• Refractive Index: 1.566
• Boiling Point: 233.2 °C at 760 mmHg
• Flash Point: 94.8 °C
• PSA: 43.84000
• Density: 1.12 g/cm³
• LogP: 0.88750
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 125.095297364
• Heavy Atom Count: 9
• Complexity: 94.3

Purity/Quality:

99% ^*data from raw suppliers

(1,3-Dimethyl-1H-pyrazol-4-yl)methylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=NN(C=C1CN)C
• Use Description: C-(1,3-DIMETHYL-1H-PYRAZOL-4-YL)-METHYLAMINE, a chemical compound, has applications in various fields. In the field of organic synthesis and medicinal chemistry, it can serve as a valuable building block for the creation of diverse organic molecules, including pharmaceuticals and agrochemicals. Its role is pivotal in the synthesis of compounds with potential pharmacological properties, enabling drug discovery and development efforts. Additionally, in academic research and organic chemistry, this compound can be employed as a reagent or intermediate for the study of chemical reactions and the development of new synthetic methodologies. Its versatility across these fields underscores its significance in drug development, chemical research, and the potential advancement of treatments for various medical conditions, ultimately contributing to healthcare and scientific knowledge.