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Molecule
ID:35193
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₇BrN₂O₂
Molecular Mass
267.07878
Exact Mass
265.96908947
Charge
0
InChI
InChI=1S/C10H7BrN2O2/c11-7-3-1-6(2-4-7)8-5-9(10(14)15)13-12-8/h1-5H,(H,12,13)(H,14,15)
InChIKey
QEOVHDPWTQAMLB-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc(cc1)c1n[nH]c(c1)C(=O)O
Isomeric Smiles
c1(cc(n[nH]1)c1ccc(cc1)Br)C(=O)O
Calculated Properties
JChem
Acid pKa
3.1672041
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
0.34756142
LogD (pH = 7.4)
-0.79439086
Log P
2.6568422
Molar Refractivity
59.2661
Polarizability
23.221266
Polar Surface Area
65.98
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Safety Information
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Physical Property
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Product Information
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Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
037965
Life Chemicals
F3250-0623
Sigma Aldrich
633704
Enamine
EN300-13028
A&J Pharmtech
AJA-O34289
Academic Data
PubChem
4737228
Names and Identifiers
IUPAC Traditional name
5-(4-bromophenyl)-2H-pyrazole-3-carboxylic acid
5-(4-bromophenyl)-1H-pyrazole-3-carboxylic acid
IUPAC name
3-(4-bromophenyl)-1H-pyrazole-5-carboxylic acid
5-(4-bromophenyl)-1H-pyrazole-3-carboxylic acid
Synonyms
3-(4-Bromophenyl)-1H-pyrazole-5-carboxylic acid
3-(4-Bromophenyl)-1H-pyrazole-5-carboxylic acid
3-(4-溴苯基)-1H-吡唑-5-羧酸
5-(4-BROMOPHENYL)-1H-PYRAZOLE-3-CARBOXYLIC ACID
Registration numbers
CAS Number
46413-66-5
890591-20-5
MDL Number
MFCD06200702
MFCD02709758
PubChem SID
24882573
160998500
PubChem CID
4737228
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
GHS Hazard statements
H302
-
H319
Source
German water hazard class
3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
22
Source
Safety Statements
36
Source
GHS Precautionary statements
P305+P351+P338
Source
GHS Signal Word
Warning
Source
European Hazard Symbols
Harmful (Xn)
Source
Physical Property
Partition Coefficient
2.896
Source
Melting Point
258-262 °C(lit.)
Source
Hydrophobicity(logP)
3.516
Source
Product Information
Purity
95+%
Source
97%
Source
95%
Source
98%
Source
Empirical Formula (Hill Notation)
C10H7BrN2O2
Source
Pharmacology Properties
Gene Information
human ... PTPN1(5770)
Source
Molecule Details
Sigma Aldrich
633704
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay