5-(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)thiophene-2-carbaldehyde

Base Information

• Chemical Name: 5-(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)thiophene-2-carbaldehyde
• CAS No.: 175202-94-5
• Molecular Formula: C10H7 F3 N2 O S
• Molecular Weight: 260.24
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID80379645
• Wikidata: Q82169541
• Mol file: 175202-94-5.mol

Synonyms:175202-94-5;2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-thiophene-5-carboxaldehyde;5-(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)thiophene-2-carbaldehyde;5-[2-methyl-5-(trifluoromethyl)pyrazol-3-yl]thiophene-2-carbaldehyde;2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]thiophene-5-carboxaldehyde;5-[1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]thiophene-2-carbaldehyde;2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]thiophene-5-carbaldehyde;SCHEMBL3616291;DTXSID80379645;MFCD00052158;2-Thiophenecarboxaldehyde,5-[1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]-;AKOS015850863;PS-7368;CS-0333848;FT-0610850;A811852;5-[1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]-2-thiophenecarbaldehyde;5-[1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]-2-thiophenecarbaldehyde, AldrichCPR

Chemical Property of 5-(1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)thiophene-2-carbaldehyde

Chemical Property:

• Vapor Pressure: 1.47E-05mmHg at 25°C
• Melting Point: 75-78oC
• Boiling Point: 366.3°C at 760 mmHg
• PKA: -1.26±0.10(Predicted)
• Flash Point: 175.4°C
• PSA: 63.13000
• Density: 1.46g/cm³
• LogP: 2.97990
• Storage Temp.: 2-8°C
• Sensitive.: Stench
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 260.02311851
• Heavy Atom Count: 17
• Complexity: 300

Purity/Quality:

98%min ^*data from raw suppliers

2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]thiophene-5-carboxaldehyde 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38-36
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1C(=CC(=N1)C(F)(F)F)C2=CC=C(S2)C=O