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850568-21-7 molecular structure
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[4-(4-methylpiperidine-1-carbonyl)phenyl]boronic acid

ChemBase ID: 75786
Molecular Formular: C13H18BNO3
Molecular Mass: 247.09792
Monoisotopic Mass: 247.13797384
SMILES and InChIs

SMILES:
B(c1ccc(cc1)C(=O)N1CCC(CC1)C)(O)O
Canonical SMILES:
OB(c1ccc(cc1)C(=O)N1CCC(CC1)C)O
InChI:
InChI=1S/C13H18BNO3/c1-10-6-8-15(9-7-10)13(16)11-2-4-12(5-3-11)14(17)18/h2-5,10,17-18H,6-9H2,1H3
InChIKey:
YPAMJFMJEPYVFW-UHFFFAOYSA-N

Cite this record

CBID:75786 http://www.chembase.cn/molecule-75786.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[4-(4-methylpiperidine-1-carbonyl)phenyl]boronic acid
IUPAC Traditional name
4-(4-methylpiperidine-1-carbonyl)phenylboronic acid
Synonyms
[4-(4-Methylpiperidine-1-carbonyl)]benzeneboronic acid
4-(4-Methyl-1-piperidinylcarbonyl)benzeneboronic acid
4-(4-METHYLPIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID
4-(4-甲基-1-哌啶基羰基)苯硼酸
CAS Number
850568-21-7
MDL Number
MFCD04115676
PubChem SID
162040704
PubChem CID
44118527

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 44118527 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors 3  H Donor 2 
LogD (pH = 5.5) 1.8359525  LogD (pH = 7.4) 1.8095402 
Log P 1.8363  Molar Refractivity 66.1659 cm3
Polarizability 26.686691 Å3 Polar Surface Area 60.77 Å2
Rotatable Bonds 2  Lipinski's Rule of Five true 
Acid pKa 8.594491 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
134-137°C expand Show data source
134-137°C 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
否 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
98% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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