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Molecule
ID:87610
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₂BrNO₃
Molecular Mass
262.10048
Exact Mass
261.00005525
Charge
0
InChI
InChI=1S/C9H11NO3.BrH/c10-13-8(9(11)12)6-7-4-2-1-3-5-7;/h1-5,8H,6,10H2,(H,11,12);1H/t8-;/m1./s1
InChIKey
YENJJZAVLSPBIZ-DDWIOCJRSA-N
Canonic Smiles
NO[C@@H](C(=O)O)Cc1ccccc1.Br
Isomeric Smiles
OC(=O)[C@@H](Cc1ccccc1)ON.Br
Calculated Properties
JChem
Acid pKa
3.4882417
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-0.4878233
LogD (pH = 7.4)
-1.9629703
Log P
0.33222634
Molar Refractivity
47.5285
Polarizability
18.598347
Polar Surface Area
72.55
Rotatable Bonds
4
Lipinski's Rule of Five
true
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Molecule Details
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Data Source
Commercial Catalog
Apollo Scientific
OR3245T
TRC
A632450
Academic Data
PubChem
44119299
Names and Identifiers
Synonyms
(2R)-2-(Aminooxy)-3-phenylpropanoic acid hydrobromide
D-alpha-Aminoxy-beta-phenylpropionic acid hydrobromide
D-α-Aminoxy-β-phenylpropionic Acid Hydrobromide, 66% ee
(R)-α-(Aminooxy)benzenepropanoic Acid Hydrobromide
IUPAC Traditional name
(2R)-2-(aminooxy)-3-phenylpropanoic acid hydrobromide
IUPAC name
(2R)-2-(aminooxy)-3-phenylpropanoic acid hydrobromide
Registration numbers
PubChem SID
162074650
PubChem CID
44119299
CAS Number
73086-98-3
MDL Number
MFCD01320369
Molecule Details
Apollo Scientific
OR3245T
Useful intermediate for the synthesis of optically active amino acids.
TRC
A632450
Phenylalanine aminoxy analog.
References
PubChem Literature
From Data Sources
•
Briggs, M.T., et al.: Bioorg. Chem., 9, 2138 (1979)
Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
Irritant
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MSDS Link
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Storage Condition
Refrigerator
Source
Physical Property
Melting Point
165-167°C
Source
152-154°C
Source
White Powder
Source
Methanol
Source
DMSO
Source
Water
Source
Product Information
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Apperance
Solubility
Certificate of Analysis