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Molecule
ID:118843
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₆N₂O₂
Molecular Mass
268.31044
Exact Mass
268.12117776
Charge
0
InChI
InChI=1S/C16H16N2O2/c17-10-14(16(19)20)9-11-7-12-3-1-5-18-6-2-4-13(8-11)15(12)18/h7-9H,1-6H2,(H,19,20)/b14-9-
InChIKey
JXENNHTVELFRHV-ZROIWOOFSA-N
Canonic Smiles
N#C/C(=C/c1cc2CCCN3c2c(c1)CCC3)/C(=O)O
Isomeric Smiles
C(=C\c1cc2c3c(c1)CCCN3CCC2)(\C(=O)O)/C#N
Calculated Properties
JChem
Acid pKa
2.7652545
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
0.5346365
LogD (pH = 7.4)
-0.44552946
Log P
1.2530572
Molar Refractivity
78.3633
Polarizability
28.453712
Polar Surface Area
64.33
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
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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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IUPAC Traditional name
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IUPAC name
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PubChem CID
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PubChem SID
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CAS Number
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MDL Number
Properties
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Physical Property
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Product Information
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Safety Information
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
Life Chemicals
F9995-0222
Sigma Aldrich
72301
Academic Data
PubChem
45497365
Names and Identifiers
Synonyms
(2Z)-2-cyano-3-(2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-9-yl)acrylic acid
9-(2-Carboxy-2-cyanovinyl)julolidine
9-([E]-2-Carboxy-2-cyanovinyl)julolidine
CCVJ
IUPAC Traditional name
(2Z)-3-{1-azatricyclo[7.3.1.0
5
,
1
3
]trideca-5,7,9(13)-trien-7-yl}-2-cyanoprop-2-enoic acid
3-{1-azatricyclo[7.3.1.0
5
,
1
3
]trideca-5,7,9(13)-trien-7-yl}-2-cyanoprop-2-enoic acid
IUPAC name
(2Z)-3-{1-azatricyclo[7.3.1.0
5
,
1
3
]trideca-5,7,9(13)-trien-7-yl}-2-cyanoprop-2-enoic acid
3-{1-azatricyclo[7.3.1.0
5
,
1
3
]trideca-5,7,9(13)-trien-7-yl}-2-cyanoprop-2-enoic acid
Registration numbers
PubChem CID
45497365
PubChem SID
162102823
24886383
CAS Number
142978-18-5
MDL Number
MFCD00274408
MFCD14584925
Molecule Details
Sigma Aldrich
72301
Application
Fluorescent probe for binding to proteins etc., quantum yield increases by decreasing free rotation: fluorescent molecular rotor.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Partition Coefficient
2.318
Source
Solubility
DMSO: soluble
Source
chloroform: soluble
Source
Fluorescence
λex 433 nm; λem 500 nm in 50 mM Tris pH 8.0; 40% glycerol
Source
Product Information
Purity
95+%
Source
≥97.0% (HPLC)
Source
Suitability
suitable for fluorescence
Source
Product Line
BioReagent
Source
Empirical Formula (Hill Notation)
C16H16N2O2
Source
Safety Information
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
H315
-
H319
-
H335
Source
P261
-
P305+P351+P338
Source
Download link
Source
Irritant (Xi)
36/37/38
Source
26
-
36
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
Warning
Source
3
Source
Source
GHS Hazard statements
GHS Precautionary statements
MSDS Link
European Hazard Symbols
Risk Statements
Safety Statements
Personal Protective Equipment
GHS Signal Word
German water hazard class