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Molecule
ID:68708
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₂O₃
Molecular Mass
180.20048
Exact Mass
180.07864424
Charge
0
InChI
InChI=1S/C10H12O3/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9,11H,6-7H2,(H,12,13)/t9-/m1/s1
InChIKey
JNJCEALGCZSIGB-SECBINFHSA-N
Canonic Smiles
O[C@@H](C(=O)O)CCc1ccccc1
Isomeric Smiles
C(=O)([C@@H](CCc1ccccc1)O)O
Calculated Properties
JChem
Acid pKa
4.1208735
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
0.23522814
LogD (pH = 7.4)
-1.4566362
Log P
1.6290655
Molar Refractivity
48.0598
Polarizability
18.833664
Polar Surface Area
57.53
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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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
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IUPAC name
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Molecular Spectra
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Sigma Aldrich
References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
074170
Sigma Aldrich
420085
56112
Bide Pharmatech
BD12035
Alfa Aesar
H52804
Academic Data
PubChem
2759328
Names and Identifiers
IUPAC name
(2R)-2-hydroxy-4-phenylbutanoic acid
Synonyms
(R)-2-Hydroxy-4-phenylbutyric acid
(R)-2-羟基-4-苯基丁酸
(R)-2-Hydroxy-4-phenylbutyric acid
(R)-(-)-2-Hydroxy-4-phenylbutyric acid
(R)-(-)-2-羟基-4-苯基丁酸
IUPAC Traditional name
(2R)-2-hydroxy-4-phenylbutanoic acid
Registration numbers
Beilstein Number
3201296
MDL Number
MFCD00192219
PubChem SID
24866310
162034438
CAS Number
29678-81-7
PubChem CID
2759328
Molecule Details
Sigma Aldrich
420085
Packaging
100 mg in glass bottle
56112
Other Notes
Chiral building block; the triflate of the corresponding ester is used for preparing ACE inhibitors1,2,3
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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Beilstein Number
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MDL Number
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PubChem SID
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CAS Number
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PubChem CID
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
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Source
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Source
TSCA Listed
false
Source
否
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
95+%
Source
99%
Source
≥99.0% (sum of enantiomers, HPLC)
Source
97%
Source
C6H5CH2CH2CH(OH)CO2H
Source
puriss.
Source
Physical Property
114-117 °C(lit.)
Source
114-117 °C
Source
114-117°C
Source
[α]20/D -9.5°, c = 2.8 in ethanol
Source
[α]20/D -9.5±1°, c = 2.8% in ethanol
Source
-9.5 (c=2.8 in ethanol)
Source
Personal Protective Equipment
German water hazard class
Purity
Linear Formula
Grade
Melting Point
Optical Rotation