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Molecule
ID:54961
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₆INO₂
Molecular Mass
297.13331
Exact Mass
297.02257676
Charge
0
InChI
InChI=1S/C9H16INO2/c1-9(2,3)13-8(12)11-5-7(4-10)6-11/h7H,4-6H2,1-3H3
InChIKey
CJVGFEARJOREHI-UHFFFAOYSA-N
Canonic Smiles
ICC1CN(C1)C(=O)OC(C)(C)C
Isomeric Smiles
N1(CC(C1)CI)C(=O)OC(C)(C)C
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.2528384
LogD (pH = 7.4)
2.2528384
Log P
2.2528384
Molar Refractivity
59.8524
Polarizability
23.60355
Polar Surface Area
29.54
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
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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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Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
Registration numbers
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PubChem CID
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MDL Number
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CAS Number
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PubChem SID
Properties
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Product 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
53249943
Commercial Catalog
Matrix Scientific
059932
Bide Pharmatech
BD167910
Names and Identifiers
IUPAC Traditional name
tert-butyl 3-(iodomethyl)azetidine-1-carboxylate
Synonyms
1-Boc-3-(iodomethyl)azetidine
tert-Butyl 3-(iodomethyl)azetidine-1-carboxylate
IUPAC name
tert-butyl 3-(iodomethyl)azetidine-1-carboxylate
Registration numbers
PubChem CID
53249943
MDL Number
MFCD09951816
CAS Number
253176-94-2
PubChem SID
162059724
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Product Information
Purity
95%
Source
95+%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay