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Molecule
ID:134666
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₁NO₃
Molecular Mass
184.16650451
Exact Mass
184.08395773
Charge
0
InChI
InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1/i5+1,8+1,9+1
InChIKey
OUYCCCASQSFEME-RGZNPSMASA-N
Canonic Smiles
O[13C](=O)[13C@H]([13CH2]c1ccc(cc1)O)N
Isomeric Smiles
c1cc(ccc1[13CH2][13C@@H]([13C](=O)O)N)O
Calculated Properties
JChem
Acid pKa
1.9998473
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-1.4884841
LogD (pH = 7.4)
-1.495157
Log P
-1.488594
Molar Refractivity
47.0972
Polarizability
18.512522
Polar Surface Area
83.55
Rotatable Bonds
3
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
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
•
IUPAC name
Registration numbers
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PubChem SID
•
PubChem CID
Properties
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Safety Information
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Physical Property
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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
Commercial Catalog
Sigma Aldrich
587842
Academic Data
PubChem
71308851
Names and Identifiers
Synonyms
L-4-羟基苯基丙氨酸-1,2,3-13C3
L-4-Hydroxyphenylalanine-1,2,3-13C3
L-Tyrosine-1,2,3-13C3
L-酪氨酸-1,2,3-13C3
IUPAC Traditional name
(2S)-2-amino-3-(4-hydroxyphenyl)(1,2,3-
1
3
C
3
)propanoic acid
IUPAC name
(2S)-2-amino-3-(4-hydroxyphenyl)(1,2,3-
1
3
C
3
)propanoic acid
Registration numbers
PubChem SID
162228942
PubChem CID
71308851
Properties
Safety Information
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
GHS Signal Word
Warning
Source
Risk Statements
36/37/38
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
MSDS Link
Download link
Source
Safety Statements
26
-
36
Source
Physical Property
Mass Shift
M+3
Source
Melting Point
300 °C (dec.)(lit.)
Source
Optical Rotation
[α]20/D -10.6°, c = 4 in 1 M HCl
Source
Product Information
Linear Formula
4-HO-C6H413CH213CH(NH2)13COOH
Source
Mol. Weight
mol wt 184.15 by atom % calculation
Source
Isotopic Purity
99 atom % 13C
Source
Molecule Details
Sigma Aldrich
587842
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay