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Molecule
ID:12188
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄BrNO₄
Molecular Mass
246.01496
Exact Mass
244.93236961
Charge
0
InChI
InChI=1S/C7H4BrNO4/c8-4-1-2-5(7(10)11)6(3-4)9(12)13/h1-3H,(H,10,11)
InChIKey
ZIRHHEZLJGORGU-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc(c(c1)[N+](=O)[O-])C(=O)O
Isomeric Smiles
c1c(cc(c(c1)C(=O)O)[N+](=O)[O-])Br
Calculated Properties
JChem
Acid pKa
1.6352308
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
-1.0249962
LogD (pH = 7.4)
-1.1873839
Log P
2.3395655
Molar Refractivity
47.2575
Polarizability
17.742582
Polar Surface Area
80.44
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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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
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RDKit
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JChem
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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MDL Number
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CAS Number
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PubChem SID
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PubChem CID
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
009241
Apollo Scientific
OR1244
Life Chemicals
F9995-0102
Sigma Aldrich
664855
TRC
B686225
Enamine
EN300-99720
Bide Pharmatech
BD10256
Alfa Aesar
H27541
A&J Pharmtech
AJA-O40305
Academic Data
PubChem
3774467
Names and Identifiers
Synonyms
4-Bromo-2-nitrobenzoic acid
5-Bromo-2-carboxynitrobenzene
4-Bromo-2-nitrobenzoic acid
4-溴-2-硝基苯甲酸
IUPAC Traditional name
4-bromo-2-nitrobenzoic acid
IUPAC name
4-bromo-2-nitrobenzoic acid
Registration numbers
MDL Number
MFCD01013599
CAS Number
99277-71-1
PubChem SID
24884696
160975495
PubChem CID
3774467
Molecule Details
Sigma Aldrich
664855
Application
Undergoes Negishi-type coupling with dimethylzinc in the presence of palladium-phosphine catalysis.1
Packaging
1, 5 g in glass bottle
TRC
B686225
4-Bromo-2-nitrobenzoic acid is an intermediate in the synthesis of Lonafarnib (L469445), a potential anticancer agent.
References
PubChem Literature
From Data Sources
•
Pellicani, R.Z., et al.: J. Med. Chem., 55, 424 (2012)
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
165-169
Source
165-169°C
Source
165-169 °C
Source
165-169°C
Source
Partition Coefficient
2.351
Source
Hydrophobicity(logP)
2.365
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Harmful
Source
TSCA Listed
false
Source
否
Source
3
Source
H302
-
H315
-
H317
-
H319
-
H335
-
H400
Source
H315
-
H319
-
H335
Source
22
-
36/37/38
-
43
-
50
Source
36/37/38
Source
2
Source
3077
Source
Harmful (Xn)
P261
-
P273
-
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
9
Source
Warning
Source
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
UN 3077 9/PG 3
Source
26
-
36/37
-
61
Source
26
-
37
Source
Product Information
Purity
97%
Source
95+%
Source
95%
Source
98%
Source
Linear Formula
(Br)C6H3(NO2)CO2H
Source
Certificate of Analysis
Download link
Source
Source
Nature polluting (N)
Source
Irritant (Xi)
Source
Source
Source
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Source
Packing Group
GHS Hazard statements
Risk Statements
German water hazard class
UN Number
European Hazard Symbols
GHS Precautionary statements
GHS Pictograms
Hazard Class
GHS Signal Word
Personal Protective Equipment
RID/ADR
Safety Statements