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Molecule
ID:108239
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₇NO₃
Molecular Mass
271.31108
Exact Mass
271.12084341
Charge
0
InChI
InChI=1S/C16H17NO3/c17-15(16(18)19)10-12-6-8-14(9-7-12)20-11-13-4-2-1-3-5-13/h1-9,15H,10-11,17H2,(H,18,19)/t15-/m0/s1
InChIKey
KAFHLONDOVSENM-HNNXBMFYSA-N
Canonic Smiles
N[C@H](C(=O)O)Cc1ccc(cc1)OCc1ccccc1
Isomeric Smiles
N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)O
Calculated Properties
JChem
Acid pKa
1.9508076
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.38191238
LogD (pH = 7.4)
0.3785746
Log P
0.3818868
Molar Refractivity
76.1921
Polarizability
29.993883
Polar Surface Area
72.55
Rotatable Bonds
6
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
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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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IUPAC Traditional name
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IUPAC name
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Product Information
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Physical Property
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Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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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
MP Biomedicals
05206647
Sigma Aldrich
855839
14010
Chemik
CHB85661
Academic Data
PubChem
725701
Names and Identifiers
Synonyms
O-BENZYL-L-TYROSINE
O-Benzyl-L-tyrosine
4-Benzyloxy-L-phenylalanine
O-苄基-L-酪氨酸
4-苄氧基-L-苯丙氨酸
H-Tyr(Bzl)-OH
IUPAC Traditional name
(2S)-2-amino-3-[4-(benzyloxy)phenyl]propanoic acid
IUPAC name
(2S)-2-amino-3-[4-(benzyloxy)phenyl]propanoic acid
Registration numbers
CAS Number
16652-64-5
PubChem SID
162095472
24848452
PubChem CID
725701
MDL Number
MFCD00002605
EC Number
240-699-1
Beilstein Number
2659642
Properties
Product Information
Certificate of Analysis
Download link
Source
Linear Formula
C6H5CH2OC6H4CH2CH(NH2)CO2H
Source
Purity
97%
Source
≥99.0% (NT)
Source
Safety Information
MSDS Link
Download link
Source
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Source
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Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Physical Property
Melting Point
259 °C (dec.)(lit.)
Source
Optical Rotation
[α]20/D -8.9°, c = 1 in acetic acid: water (4:1)
Source
[α]20/D -9.5±1°, c = 1% in acetic acid: water (4:1)
Source
Pharmacology Properties
Gene Information
human ... PPARG(5468)
Source
Molecule Details
MP Biomedicals
05206647
MP Biomedicals Rare Chemical collection
Sigma Aldrich
855839
Packaging
5 g in glass bottle
14010
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem SID
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MDL Number
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EC Number
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