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Molecule
ID:38743
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₂₃NO₆
Molecular Mass
289.32482
Exact Mass
289.15253746
Charge
0
InChI
InChI=1S/C13H23NO6/c1-13(2,3)20-12(19)14-9(11(17)18)7-5-4-6-8-10(15)16/h9H,4-8H2,1-3H3,(H,14,19)(H,15,16)(H,17,18)/t9-/m1/s1
InChIKey
WZVLJRPOVUCTFZ-SECBINFHSA-N
Canonic Smiles
OC(=O)[C@H](NC(=O)OC(C)(C)C)CCCCCC(=O)O
Isomeric Smiles
C(CCCC[C@H](C(=O)O)NC(=O)OC(C)(C)C)C(=O)O
Calculated Properties
JChem
Acid pKa
3.6715682
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-1.0735303
LogD (pH = 7.4)
-4.3635755
Log P
1.8939414
Molar Refractivity
69.9637
Polarizability
27.76085
Polar Surface Area
112.93
Rotatable Bonds
10
Lipinski's Rule of Five
true
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Related Proteins
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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
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IUPAC Traditional name
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IUPAC name
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MDL Number
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
12879022
Commercial Catalog
Sigma Aldrich
672092
Matrix Scientific
041635
Names and Identifiers
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]octanedioic acid
Synonyms
Boc-D-Asu-OH
(R)-2-(Boc-氨基)辛二酸
(R)-2-(Boc-amino)octanedioic acid
Boc-D-2-aminosuberic acid
Boc-D-2-氨基辛二酸
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}octanedioic acid
Registration numbers
CAS Number
75113-71-2
MDL Number
MFCD01317723
PubChem SID
161002050
PubChem CID
12879022
Molecule Details
Sigma Aldrich
672092
Packaging
1 g in glass bottle
250 mg in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
German water hazard class
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
C13H23NO6
Source
ee: ≥99% (GC)
Source
≥96.5% (TLC)
Source
97%
Source
Personal Protective Equipment
Empirical Formula (Hill Notation)
Optical Purity
Purity