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Molecule
ID:86921
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀O
Molecular Mass
134.1751
Exact Mass
134.07316494
Charge
0
InChI
InChI=1S/C9H10O/c1-7-3-4-9(6-10)5-8(7)2/h3-6H,1-2H3
InChIKey
POQJHLBMLVTHAU-UHFFFAOYSA-N
Canonic Smiles
O=Cc1ccc(c(c1)C)C
Isomeric Smiles
O=Cc1cc(c(cc1)C)C
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.712591
LogD (pH = 7.4)
2.712591
Log P
2.712591
Molar Refractivity
42.7244
Polarizability
15.760297
Polar Surface Area
17.07
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
•
Commercial Catalog
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Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC name
•
IUPAC Traditional name
Registration numbers
Properties
•
Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR30113
Sigma Aldrich
493856
Enamine
EN300-22064
Alfa Aesar
A15388
Academic Data
PubChem
22278
Names and Identifiers
Synonyms
3,4-Dimethylbenzaldehyde
4-Formyl-o-xylene
3,4-Dimethylbenzaldehyde
3,4-二甲基苯甲醛
IUPAC name
3,4-dimethylbenzaldehyde
IUPAC Traditional name
3,4-dimethylbenzaldehyde
Registration numbers
CAS Number
5973-71-7
MDL Number
MFCD00016612
PubChem SID
24872864
162074037
EC Number
227-770-2
PubChem CID
22278
Beilstein Number
1634270
Molecule Details
Sigma Aldrich
493856
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
EC Number
•
PubChem CID
•
Beilstein Number
Properties
Physical Property
Density
1.012
Source
1.012 g/mL at 25 °C(lit.)
Source
1.017
Source
Boiling Point
102-104°C/15mm
Source
226 °C(lit.)
Source
226°C
Source
Refractive Index
1.551
Source
n20/D 1.551(lit.)
Source
1.5510
Source
Melting Point
223-226°C
Source
102 - 104°C
Source
Hydrophobicity(logP)
2.443
Source
Safety Information
Storage Warning
Irritant/Air Sensitive/Store under Argon
Source
Air Sensitive
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
MSDS Link
Download link
Source
German water hazard class
3
Source
是
Source
Product Information
Linear Formula
(CH3)2C6H3CHO
Source
Purity
98%
Source
95%
Source
97%
Source
TSCA Listed