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Molecule
ID:64688
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₂₀N₂O₃
Molecular Mass
216.2774
Exact Mass
216.14739251
Charge
0
InChI
InChI=1S/C10H20N2O3/c1-10(2,3)15-9(14)12-5-4-11-8(6-12)7-13/h8,11,13H,4-7H2,1-3H3/t8-/m1/s1
InChIKey
NSILYQWHARROMG-MRVPVSSYSA-N
Canonic Smiles
OC[C@@H]1NCCN(C1)C(=O)OC(C)(C)C
Isomeric Smiles
C(=O)(N1C[C@@H](NCC1)CO)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
15.078465
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-1.8545258
LogD (pH = 7.4)
-0.32372928
Log P
-0.075948715
Molar Refractivity
56.4064
Polarizability
22.50289
Polar Surface Area
61.8
Rotatable Bonds
3
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
Calculated Properties
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RDKit
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IUPAC name
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IUPAC Traditional name
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PubChem SID
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PubChem CID
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Safety Information
Related Proteins
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
24820286
Commercial Catalog
Matrix Scientific
070016
Bide Pharmatech
BD33012
Names and Identifiers
Synonyms
(R)-1-Boc-3-(Hydroxymethyl)piperazine
IUPAC name
tert-butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate
IUPAC Traditional name
tert-butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate
Registration numbers
MDL Number
MFCD05863888
CAS Number
278788-66-2
PubChem SID
162030427
PubChem CID
24820286
Properties
Product Information
Purity
98%
Source
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
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Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay