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Molecule
ID:38319
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₂₁BrN₂O₃
Molecular Mass
369.25354
Exact Mass
368.07355454
Charge
0
InChI
InChI=1S/C16H21BrN2O3/c1-16(2,3)22-15(21)19-8-6-18(7-9-19)14-10-13(17)5-4-12(14)11-20/h4-5,10-11H,6-9H2,1-3H3
InChIKey
VUYPBCWARJBGRT-UHFFFAOYSA-N
Canonic Smiles
O=Cc1ccc(cc1N1CCN(CC1)C(=O)OC(C)(C)C)Br
Isomeric Smiles
C(=O)c1c(cc(cc1)Br)N1CCN(CC1)C(=O)OC(C)(C)C
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
3.3098092
LogD (pH = 7.4)
3.3098094
Log P
3.3098094
Molar Refractivity
90.4439
Polarizability
33.945827
Polar Surface Area
49.85
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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Properties
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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 CID
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PubChem SID
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MDL Number
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
46737204
Commercial Catalog
Matrix Scientific
041143
Names and Identifiers
Synonyms
2-(4-Boc-piperazino-1-yl)-4-bromobenzaldehyde
IUPAC name
tert-butyl 4-(5-bromo-2-formylphenyl)piperazine-1-carboxylate
IUPAC Traditional name
tert-butyl 4-(5-bromo-2-formylphenyl)piperazine-1-carboxylate
Registration numbers
PubChem CID
46737204
PubChem SID
161001626
MDL Number
MFCD11849903
Properties
Safety Information
MSDS Link
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay