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Molecule
ID:38960
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₁₈N₂O₄
Molecular Mass
290.31442
Exact Mass
290.12665707
Charge
0
InChI
InChI=1S/C15H18N2O4/c1-15(2,3)21-14(20)17-12(13(18)19)8-10-5-4-6-11(7-10)9-16/h4-7,12H,8H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1
InChIKey
FDQDHMZKOPOWFE-GFCCVEGCSA-N
Canonic Smiles
N#Cc1cccc(c1)C[C@H](C(=O)O)NC(=O)OC(C)(C)C
Isomeric Smiles
c1c(cc(cc1)C[C@H](C(=O)O)NC(=O)OC(C)(C)C)C#N
Calculated Properties
JChem
Acid pKa
2.5963087
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-0.38615525
LogD (pH = 7.4)
-1.0811629
Log P
2.4258087
Molar Refractivity
75.7109
Polarizability
29.34845
Polar Surface Area
99.42
Rotatable Bonds
6
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
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
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Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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PubChem SID
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CAS Number
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MDL Number
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PubChem CID
Properties
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Safety Information
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Product 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
Academic Data
PubChem
7021063
Commercial Catalog
Sigma Aldrich
14985
Matrix Scientific
041858
Names and Identifiers
Synonyms
Boc-3-cyano-D-phenylalanine
Boc-D-3-氰基苯丙氨酸
Boc-D-Phe(3-CN)-OH
Boc-3-cyano-D-phenylalanine
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(3-cyanophenyl)propanoic acid
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]-3-(3-cyanophenyl)propanoic acid
Registration numbers
PubChem SID
24848979
161002267
CAS Number
205445-56-3
MDL Number
MFCD00797561
PubChem CID
7021063
Molecule Details
Sigma Aldrich
14985
Packaging
5 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
≥98.0% (HPLC)
Source
C15H18N2O4
Source
German water hazard class
Purity
Empirical Formula (Hill Notation)