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Molecule
ID:70831
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₉NO₃
Molecular Mass
119.11916
Exact Mass
119.05824315
Charge
0
InChI
InChI=1S/C4H9NO3/c5-2-1-3(6)4(7)8/h3,6H,1-2,5H2,(H,7,8)
InChIKey
IVUOMFWNDGNLBJ-UHFFFAOYSA-N
Canonic Smiles
NCCC(C(=O)O)O
Isomeric Smiles
C(=O)(C(CCN)O)O
Calculated Properties
JChem
Acid pKa
3.682898
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-3.8336527
LogD (pH = 7.4)
-3.8297465
Log P
-3.828955
Molar Refractivity
26.9064
Polarizability
10.868561
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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Quote
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General Information
Calculated Properties
•
RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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CAS Number
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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
Matrix Scientific
076405
Enamine
EN300-85732
Bide Pharmatech
BD220224
A&J Pharmtech
AJA-O2115
Academic Data
PubChem
26062
Names and Identifiers
IUPAC Traditional name
4-amino-2-hydroxybutanoic acid
IUPAC name
4-amino-2-hydroxybutanoic acid
Synonyms
4-Amino-2-hydroxybutanoic acid
Registration numbers
CAS Number
13477-53-7
MDL Number
MFCD00797835
PubChem CID
26062
PubChem SID
162036540
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
95+%
Source
95%
Source
97%
Source
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
false
Source
Physical Property
-4.362
Source
196 - 206°C
Source
TSCA Listed
Hydrophobicity(logP)
Melting Point