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Molecule
ID:67641
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/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m1/s1
InChIKey
UKAUYVFTDYCKQA-GSVOUGTGSA-N
Canonic Smiles
OCC[C@H](C(=O)O)N
Isomeric Smiles
C(=O)([C@H](N)CCO)O
Calculated Properties
JChem
Acid pKa
2.2233198
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-3.8276682
LogD (pH = 7.4)
-3.8344793
Log P
-3.8277326
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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General Information
Calculated Properties
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RDKit
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JChem
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IUPAC name
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IUPAC Traditional name
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Synonyms
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Product 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
Shanghai Lingjing
113
Sigma Aldrich
H4021
377961
53595
Matrix Scientific
073077
Enamine
EN300-50993
Academic Data
PubChem
2724170
Names and Identifiers
IUPAC name
(2R)-2-amino-4-hydroxybutanoic acid
IUPAC Traditional name
D-homoserine
Synonyms
D-Homoserine
D-高丝氨酸
(R)-(+)-2-氨基-4-羟基丁酸
D-Homoserine
(R)-(+)-2-Amino-4-hydroxybutyric acid
(2R)-2-amino-4-hydroxybutanoic acid
Registration numbers
MDL Number
MFCD00077786
CAS Number
6027-21-0
Beilstein Number
1721680
PubChem SID
162033376
24895614
PubChem CID
2724170
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
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Source
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Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
Purity
95+%
Source
98%
Source
≥99.0% (CHN)
Source
95%
Source
Optical Purity
ee: 97% (GLC)
Source
Linear Formula
HOCH2CH2CH(NH2)CO2H
Source
Grade
puriss.
Source
Physical Property
Melting Point
205 °C (dec.)(lit.)
Source
205 °C (dec.)
Source
182 - 184°C
Source
Optical Rotation
[α]20/D +9°, c = 5 in H2O
Source
[α]20/D +9.0±1°, c = 2% in H2O
Source
Hydrophobicity(logP)
-3.116
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
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MDL Number
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CAS Number
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Beilstein Number
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PubChem SID
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