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Molecule
ID:22410
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₃IN₂O₂
Molecular Mass
344.14829
Exact Mass
344.00217567
Charge
0
InChI
InChI=1S/C12H13IN2O2/c1-12(2,3)17-11(16)15-9-7-5-4-6-8(9)10(13)14-15/h4-7H,1-3H3
InChIKey
DHNSGIOEVGLLOI-UHFFFAOYSA-N
Canonic Smiles
Ic1nn(c2c1cccc2)C(=O)OC(C)(C)C
Isomeric Smiles
n1c(c2c(n1C(=O)OC(C)(C)C)cccc2)I
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
3.2508998
LogD (pH = 7.4)
3.2508998
Log P
3.2508998
Molar Refractivity
73.8432
Polarizability
29.788958
Polar Surface Area
44.12
Rotatable Bonds
2
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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IUPAC Traditional name
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IUPAC name
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PubChem SID
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PubChem CID
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Product Information
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Key Organics
SS-4437
Matrix Scientific
024800
Bide Pharmatech
BD161370
A&J Pharmtech
AJA-O129
Academic Data
PubChem
11473390
Names and Identifiers
IUPAC Traditional name
tert-butyl 3-iodoindazole-1-carboxylate
Synonyms
1-Boc-3-iodoindazole
1-Boc-3-Iodo-1H-indazole
tert-butyl 3-iodo-1H-indazole-1-carboxylate
IUPAC name
tert-butyl 3-iodo-1H-indazole-1-carboxylate
Registration numbers
CAS Number
290368-00-2
MDL Number
MFCD09835520
PubChem SID
160985717
PubChem CID
11473390
Properties
Safety Information
MSDS Link
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Source
TSCA Listed
false
Source
Product Information
Purity
98%
Source
>97%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay