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Molecule
ID:130615
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₉H₃₈
Molecular Mass
266.50502
Exact Mass
266.29735122
Charge
0
InChI
InChI=1S/C19H38/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(2)3/h13-14,19H,4-12,15-18H2,1-3H3/b14-13-
InChIKey
XDBKLFODBADBED-YPKPFQOOSA-N
Canonic Smiles
CCCCCCCCCC/C=C\CCCCC(C)C
Isomeric Smiles
CCCCCCCCCC/C=C\CCCCC(C)C
Calculated Properties
JChem
H Acceptors
0
H Donor
0
LogD (pH = 5.5)
8.391059
LogD (pH = 7.4)
8.391059
Log P
8.391059
Molar Refractivity
90.2854
Polarizability
35.610783
Polar Surface Area
0.0
Rotatable Bonds
14
Lipinski's Rule of Five
false
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
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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
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Synonyms
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IUPAC Traditional name
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IUPAC name
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
M5773
Academic Data
PubChem
6242671
Names and Identifiers
Synonyms
顺-2-甲基-7-十八烯
cis-2-Methyl-7-octadecene
IUPAC Traditional name
(7Z)-2-methyloctadec-7-ene
IUPAC name
(7Z)-2-methyloctadec-7-ene
Registration numbers
CAS Number
35354-39-3
MDL Number
MFCD00049084
PubChem SID
24897043
162224893
PubChem CID
6242671
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves
Source
Storage Temperature
2-8°C
Source
German water hazard class
3
Source
Product Information
Purity
~95%
Source
Molecule Details
Sigma Aldrich
M5773
Biochem/physiol Actions
信息素抑制剂。
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay