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Molecule
ID:10023
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₂BNO₄
Molecular Mass
209.00688
Exact Mass
209.08593827
Charge
0
InChI
InChI=1S/C9H12BNO4/c11-8(9(12)13)5-6-1-3-7(4-2-6)10(14)15/h1-4,8,14-15H,5,11H2,(H,12,13)/t8-/m0/s1
InChIKey
NFIVJOSXJDORSP-QMMMGPOBSA-N
Canonic Smiles
OC(=O)[C@H](Cc1ccc(cc1)B(O)O)N
Isomeric Smiles
O=C([C@@H](N)Cc1ccc(cc1)B(O)O)O
Calculated Properties
JChem
Acid pKa
1.6505953
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-2.0806193
LogD (pH = 7.4)
-2.1028657
Log P
-2.080522
Molar Refractivity
49.6618
Polarizability
21.12036
Polar Surface Area
103.78
Rotatable Bonds
4
Lipinski's Rule of Five
true
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Related Proteins
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General Information
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IUPAC name
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Data Source
Academic Data
PubChem
150315
Commercial Catalog
Matrix Scientific
006759
Sigma Aldrich
17755
Names and Identifiers
Synonyms
4-Borono-L-phenylalanine
4-Borono-L-phenylalanine
L-BPA
4-硼-L-苯丙氨酸
4-Dihydroxyboryl-L-phenylalanine
4-二羟基氧硼基-L-苯丙氨酸
IUPAC name
(2S)-2-amino-3-[4-(dihydroxyboranyl)phenyl]propanoic acid
IUPAC Traditional name
(2S)-2-amino-3-[4-(dihydroxyboranyl)phenyl]propanoic acid
Registration numbers
CAS Number
76410-58-7
MDL Number
MFCD01075172
Beilstein Number
4458616
PubChem SID
24850368
160973330
PubChem CID
150315
Properties
Product Information
Purity
97%
Source
≥95.0% (HPLC)
Source
Empirical Formula (Hill Notation)
C9H12BNO4
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
European Hazard Symbols
Irritant (Xi)
Source
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
GHS Hazard statements
H315
-
H319
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H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Storage Temperature
2-8°C
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
German water hazard class
3
Source
Molecule Details
Sigma Aldrich
17755
Other Notes
Tyrosine analogue; employed for treatment of melanom cells by boron neutron capture therapy1
Packaging
250 mg in poly bottle
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Bioactivity
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