Home > Compound List > Compound details
874289-11-9 molecular structure
click picture or here to close

[4-(cyclohexylcarbamoyl)-3-fluorophenyl]boronic acid

ChemBase ID: 96911
Molecular Formular: C13H17BFNO3
Molecular Mass: 265.0883832
Monoisotopic Mass: 265.12855203
SMILES and InChIs

SMILES:
B(c1ccc(c(c1)F)C(=O)NC1CCCCC1)(O)O
Canonical SMILES:
O=C(c1ccc(cc1F)B(O)O)NC1CCCCC1
InChI:
InChI=1S/C13H17BFNO3/c15-12-8-9(14(18)19)6-7-11(12)13(17)16-10-4-2-1-3-5-10/h6-8,10,18-19H,1-5H2,(H,16,17)
InChIKey:
GUPNXIZRUYJZEV-UHFFFAOYSA-N

Cite this record

CBID:96911 http://www.chembase.cn/molecule-96911.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[4-(cyclohexylcarbamoyl)-3-fluorophenyl]boronic acid
IUPAC Traditional name
4-(cyclohexylcarbamoyl)-3-fluorophenylboronic acid
Synonyms
4-Cyclohexylcarbamoyl-3-fluorobenzeneboronic acid
(4-(Cyclohexylcarbamoyl)-3-fluorophenyl)boronic acid
4-(Cyclohexylcarbamoyl)-3-fluorobenzeneboronic acid 95%
4-环己基氨甲酰基-3-氟苯硼酸
CAS Number
874289-11-9
MDL Number
MFCD08436036
PubChem SID
162083555
PubChem CID
44717481

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 44717481 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.469227  H Acceptors
H Donor LogD (pH = 5.5) 2.2615366 
LogD (pH = 7.4) 2.2266479  Log P 2.262 
Molar Refractivity 65.8092 cm3 Polarizability 26.393185 Å3
Polar Surface Area 69.56 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
157-159°C expand Show data source
157-159°C expand Show data source
Storage Warning
Irritant/Keep Cold expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-37-60 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305+P351+P338-P302+P352-P321-P405-P501A expand Show data source
Purity
95% expand Show data source
95+% 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