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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 H Donor
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 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
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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