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Molecule
ID:69673
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇BrO₂
Molecular Mass
215.04398
Exact Mass
213.96294146
Charge
0
InChI
InChI=1S/C8H7BrO2/c1-11-8-4-7(9)3-2-6(8)5-10/h2-5H,1H3
InChIKey
YMXQYZABFWVXEK-UHFFFAOYSA-N
Canonic Smiles
COc1cc(Br)ccc1C=O
Isomeric Smiles
C(=O)c1c(cc(cc1)Br)OC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.2968295
LogD (pH = 7.4)
2.2968295
Log P
2.2968295
Molar Refractivity
46.728
Polarizability
17.617369
Polar Surface Area
26.3
Rotatable Bonds
2
Lipinski's Rule of Five
true
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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
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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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Names and Identifiers
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IUPAC name
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IUPAC Traditional 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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Product Information
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Physical Property
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Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
11053041
Commercial Catalog
Sigma Aldrich
661880
Matrix Scientific
075170
Chemik
CHB18538
Enamine
EN300-126205
Bide Pharmatech
BD94900
A&J Pharmtech
AJA-O24325
Names and Identifiers
IUPAC name
4-bromo-2-methoxybenzaldehyde
IUPAC Traditional name
4-bromo-2-methoxybenzaldehyde
Synonyms
4-Bromo-2-methoxybenzaldehyde
4-Bromo-2-methoxybenzaldehyde
4-溴-2-甲氧基苯甲醛
Registration numbers
CAS Number
43192-33-2
MDL Number
MFCD08276823
PubChem SID
162035399
24884552
PubChem CID
11053041
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
German water hazard class
2
Source
GHS Hazard statements
H302
Source
GHS Signal Word
Warning
Source
European Hazard Symbols
Harmful (Xn)
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
Product Information
Purity
95+%
Source
97%
Source
95%
Source
98%
Source
Empirical Formula (Hill Notation)
C8H7BrO2
Source
Physical Property
Melting Point
67-71 °C
Source
68 - 70°C
Source
Hydrophobicity(logP)
2.679
Source
Molecule Details
Sigma Aldrich
661880
Application
Building block in the synthesis of a nonacid degradable linker for solid-phase synthesis.1
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay