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913835-70-8 molecular structure
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[4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]boronic acid

ChemBase ID: 87656
Molecular Formular: C9H9BN2O3
Molecular Mass: 203.99036
Monoisotopic Mass: 204.07062256
SMILES and InChIs

SMILES:
B(c1ccc(cc1)c1nnc(o1)C)(O)O
Canonical SMILES:
OB(c1ccc(cc1)c1nnc(o1)C)O
InChI:
InChI=1S/C9H9BN2O3/c1-6-11-12-9(15-6)7-2-4-8(5-3-7)10(13)14/h2-5,13-14H,1H3
InChIKey:
SPSKFVHUUJWUPB-UHFFFAOYSA-N

Cite this record

CBID:87656 http://www.chembase.cn/molecule-87656.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]boronic acid
IUPAC Traditional name
4-(5-methyl-1,3,4-oxadiazol-2-yl)phenylboronic acid
Synonyms
2-(4-Boronophenyl)-5-methyl-1,3,4-oxadiazole
4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzeneboronic acid 98%
4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzeneboronic acid
4-(5-甲基-1,3,4-恶二唑-2-基)苯硼酸
CAS Number
913835-70-8
MDL Number
MFCD08436062
PubChem SID
162074696
PubChem CID
44119343

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 44119343 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.527822  H Acceptors
H Donor LogD (pH = 5.5) 0.6816949 
LogD (pH = 7.4) 0.65105474  Log P 0.6821 
Molar Refractivity 61.0714 cm3 Polarizability 20.700756 Å3
Polar Surface Area 79.38 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
188-190°C expand Show data source
188-190°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
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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