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Molecule
ID:102308
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₂₃NO₅
Molecular Mass
249.30402
Exact Mass
249.15762284
Charge
0
InChI
InChI=1S/C11H21NO4.H2O/c1-7(2)6-8(9(13)14)12-10(15)16-11(3,4)5;/h7-8H,6H2,1-5H3,(H,12,15)(H,13,14);1H2/t8-;/m0./s1
InChIKey
URQQEIOTRWJXBA-QRPNPIFTSA-N
Canonic Smiles
CC(C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)C.O
Isomeric Smiles
O.CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)O
Calculated Properties
JChem
Acid pKa
4.1984906
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
0.8473822
LogD (pH = 7.4)
-0.86698675
Log P
2.1674962
Molar Refractivity
59.0439
Polarizability
23.466265
Polar Surface Area
75.63
Rotatable Bonds
6
Lipinski's Rule of Five
true
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Molecule Details
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General Information
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MP Biomedicals
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From Data Sources
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Data Source
Commercial Catalog
MP Biomedicals
02101073
Alfa Aesar
A10647
Academic Data
PubChem
12373896
Names and Identifiers
IUPAC Traditional name
(2S)-2-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid hydrate
Synonyms
N-α-t-BOC-L-LEUCINE HYDRATE
N-(tert-Butoxycarbonyl)-L-leucine hydrate
Boc-Leu-OH.xH2O
N-Boc-L-亮氨酸水合物
N-Boc-L-leucine hydrate
IUPAC name
(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methylpentanoic acid hydrate
Registration numbers
EC Number
236-073-2
CAS Number
13139-15-6
PubChem SID
162088394
PubChem CID
12373896
Beilstein Number
1711814
MDL Number
MFCD00066067
Molecule Details
MP Biomedicals
02101073
Hydrate
Crystalline
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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EC Number
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CAS Number
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PubChem SID
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PubChem CID
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Beilstein Number
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MDL Number
Properties
Safety Information
Storage Condition
0°C
Source
MSDS Link
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TSCA Listed
是
Source
Product Information
Certificate of Analysis
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Source
99%
Source
Physical Property
84-87°C
Source
-25 (c=2 in acetic acid)
Source
Purity
Melting Point
Optical Rotation