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Molecule
ID:125055
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₃NO₄
Molecular Mass
187.19312
Exact Mass
187.0844579
Charge
0
InChI
InChI=1S/C8H13NO4/c1-8(2,3)13-7(11)9-5-4-12-6(5)10/h5H,4H2,1-3H3,(H,9,11)/t5-/m0/s1
InChIKey
HRJDEHQWXAPGBG-YFKPBYRVSA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@H]1COC1=O
Isomeric Smiles
O=C(OC(C)(C)C)N[C@@H]1C(=O)OC1
Calculated Properties
JChem
Acid pKa
13.022061
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.5309472
LogD (pH = 7.4)
0.5309463
Log P
0.5309472
Molar Refractivity
43.4218
Polarizability
17.529295
Polar Surface Area
64.63
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
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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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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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PubChem SID
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PubChem CID
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CAS Number
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MDL Number
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
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
105
Sigma Aldrich
713473
TRC
B667390
Bide Pharmatech
BD141700
Academic Data
PubChem
2763194
Names and Identifiers
Synonyms
N-Boc-L-serine beta-Lactone
(S)-N-(叔丁氧羰基)-3-氨基-2-丙醇酸丙酯
N-(tert-Butoxycarbonyl)-L-serine β-lactone
S-N-Boc-丝氨酸内酯
N-Boc-L-serine β-lactone
N-叔丁氧羰基-L-丝氨酸 β-内酯
Vederas β-内酯 (Boc)
N-(叔丁氧羰基)-L-丝氨酸 β-内酯
(S)-N-(tert-Butoxycarbonyl)-3-amino-2-oxetanone
Vederas β-lactone (Boc)
Boc-L-Serine-beta-Lactone
[(3S)-2-oxo-3-oxetanyl]-1,1-dimethylethyl Ester Carbamic Acid
N-Boc L-Serine β-Lactone
IUPAC Traditional name
tert-butyl N-[(3S)-2-oxooxetan-3-yl]carbamate
IUPAC name
tert-butyl N-[(3S)-2-oxooxetan-3-yl]carbamate
Registration numbers
PubChem SID
162219405
PubChem CID
2763194
CAS Number
98541-64-1
MDL Number
MFCD01318414
Properties
Physical Property
Vapor Pressure
0.000349mmHg at 25°C
Source
Boiling Point
319°C at 760 mmHg
Source
Density
1.18g/cm
3
Source
Flash Point
146.7°C
Source
Optical Rotation
[α]/D -25.5±1.5°, c = 1 in acetonitrile
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Storage Temperature
2-8°C
Source
Product Information
Purity
≥96.0% (GC)
Source
95+%
Source
Empirical Formula (Hill Notation)
C8H13NO4
Source
Certificate of Analysis
Download link
Source
Molecule Details
Sigma Aldrich
713473
Packaging
500 mg in glass bottle
TRC
B667390
An important β-lactone inhibitor.
References
PubChem Literature
From Data Sources
•
Kaddis, F., et al.: Pharmacol. Biochem. Behav., 46, 703 (1992)
•
Willins, D.L., et al.: J. Pharmacol. Exp. Ther., 260. 1145 (1992)
Bioactivity
PubChem BioAssay