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Molecule
ID:92811
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₉BrO
Molecular Mass
201.06046
Exact Mass
199.98367691
Charge
0
InChI
InChI=1S/C8H9BrO/c1-2-10-8-6-4-3-5-7(8)9/h3-6H,2H2,1H3
InChIKey
JVEQWIQHHWNMQX-UHFFFAOYSA-N
Canonic Smiles
CCOc1ccccc1Br
Isomeric Smiles
O(c1c(cccc1)Br)CC
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.9411352
LogD (pH = 7.4)
2.9411352
Log P
2.9411352
Molar Refractivity
44.8926
Polarizability
17.471752
Polar Surface Area
9.23
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
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
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
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
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR9597
Sigma Aldrich
713759
Enamine
EN300-65438
Bide Pharmatech
BD72266
Academic Data
PubChem
68500
Names and Identifiers
Synonyms
1-Bromo-2-ethoxybenzene
2-Bromophenetole
2-Bromophenetole
o-Bromophenetole
1-bromo-2-ethoxybenzene
邻溴苯乙醚
1-溴-2-乙氧基苯
2-溴乙氧基苯
2-溴苯乙醚
1-Bromo-2-ethoxy-benzene
2-Bromoethoxybenzene
IUPAC name
1-bromo-2-ethoxybenzene
IUPAC Traditional name
1-bromo-2-ethoxybenzene
Registration numbers
CAS Number
583-19-7
MDL Number
MFCD00061092
EC Number
209-501-0
Beilstein Number
2043678
PubChem SID
162079509
PubChem CID
68500
Molecule Details
Sigma Aldrich
713759
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
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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Beilstein Number
•
PubChem SID
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PubChem CID
Properties
Safety Information
Storage Warning
Irritant
Source
MSDS Link
Download link
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
≥97.0% (GC)
Source
95%
Source
95+%
Source
C8H9BrO
Source
Physical Property
3.363
Source
Purity
Empirical Formula (Hill Notation)
Hydrophobicity(logP)