Home > Compound List > Compound details
MFCD20265234 molecular structure
click picture or here to close

[3-fluoro-5-(4-methylpiperidine-1-carbonyl)phenyl]boronic acid

ChemBase ID: 298629
Molecular Formular: C13H17BFNO3
Molecular Mass: 265.0883832
Monoisotopic Mass: 265.12855203
SMILES and InChIs

SMILES:
B(c1cc(cc(c1)F)C(=O)N1CCC(CC1)C)(O)O
Canonical SMILES:
CC1CCN(CC1)C(=O)c1cc(F)cc(c1)B(O)O
InChI:
InChI=1S/C13H17BFNO3/c1-9-2-4-16(5-3-9)13(17)10-6-11(14(18)19)8-12(15)7-10/h6-9,18-19H,2-5H2,1H3
InChIKey:
WAWIUKFKZSQNOM-UHFFFAOYSA-N

Cite this record

CBID:298629 http://www.chembase.cn/molecule-298629.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[3-fluoro-5-(4-methylpiperidine-1-carbonyl)phenyl]boronic acid
IUPAC Traditional name
3-fluoro-5-(4-methylpiperidine-1-carbonyl)phenylboronic acid
Synonyms
3-Fluoro-5-(4-methyl-1-piperidinylcarbonyl)phenylboronic acid
3-Fluoro-5-(4-methyl-1-piperidinylcarbonyl)benzeneboronic acid
3-氟-5-(4-甲基-1-哌啶甲酰胺基)苯硼酸
MDL Number
MFCD20265234
PubChem SID
180684160
PubChem CID
73995749

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Alfa Aesar
H54310 external link Add to cart Please log in.
Data Source Data ID
PubChem 73995749 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.443603  H Acceptors
H Donor LogD (pH = 5.5) 1.9753083 
LogD (pH = 7.4) 1.9383898  Log P 1.9758 
Molar Refractivity 66.3823 cm3 Polarizability 26.390865 Å3
Polar Surface Area 60.77 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
European Hazard Symbols
X expand Show data source
Risk Statements
22-36/37/38 expand Show data source
Safety Statements
26-37 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS Hazard statements
H301-H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P301+P310-P305+P351+P338-P302+P352-P405-P501 expand Show data source
Purity
97% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle