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Molecule
ID:52890
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₆BrNO₂
Molecular Mass
216.03204
Exact Mass
214.95819044
Charge
0
InChI
InChI=1S/C7H6BrNO2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,9H2,(H,10,11)
InChIKey
BNNICQAVXPXQAH-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc(c(c1)N)C(=O)O
Isomeric Smiles
c1cc(c(cc1Br)N)C(=O)O
Calculated Properties
JChem
Acid pKa
4.724331
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.3470687
LogD (pH = 7.4)
-0.4264635
Log P
2.2206554
Molar Refractivity
45.6374
Polarizability
16.777214
Polar Surface Area
63.32
Rotatable Bonds
1
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
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
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Commercial Catalog
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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
Properties
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Safety Information
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Product Information
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Physical Property
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
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
057593
Apollo Scientific
OR13732
Life Chemicals
F9995-0103
Sigma Aldrich
664863
Chemik
CHB43200
Enamine
EN300-42681
Bide Pharmatech
BD4525
Academic Data
PubChem
88691
Names and Identifiers
IUPAC Traditional name
2-amino-4-bromobenzoic acid
IUPAC name
2-amino-4-bromobenzoic acid
Synonyms
2-Amino-4-bromobenzoic acid
2-氨基-4-溴苯甲酸
2-Amino-4-bromobenzoic acid
5-Bromo-2-carboxyaniline
4-Bromoanthranilic acid
Registration numbers
CAS Number
20776-50-5
MDL Number
MFCD03618454
EC Number
244-025-7
PubChem SID
24884697
162057653
PubChem CID
88691
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Toxic/Harmful/Irritant/Light Sensitive
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
GHS Hazard statements
H301
-
H319
Source
Risk Statements
22
Source
GHS Precautionary statements
P301+P310
-
P305+P351+P338
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
European Hazard Symbols
Harmful (Xn)
Source
RID/ADR
UN 2811 6.1/PG 3
Source
GHS Signal Word
Danger
Source
UN Number
2811
Source
Packing Group
3
Source
Hazard Class
6.1
Source
German water hazard class
3
Source
Safety Statements
36/37
Source
Product Information
Purity
97%
Source
95+%
Source
95%
Source
Linear Formula
(H2N)C6H3(Br)CO2H
Source
Physical Property
Melting Point
230-234°C
Source
230-234 °C
Source
222 - 224°C
Source
Partition Coefficient
1.744
Source
Hydrophobicity(logP)
2.198
Source
Molecule Details
Sigma Aldrich
664863
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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MDL Number
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EC Number
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PubChem SID
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PubChem CID