Home > Compound List > Compound details
871332-76-2 molecular structure
click picture or here to close

(4-chloro-3-methylphenyl)boronic acid; isocyanatomethane

ChemBase ID: 298177
Molecular Formular: C9H11BClNO3
Molecular Mass: 227.45254
Monoisotopic Mass: 227.0520513
SMILES and InChIs

SMILES:
B(c1ccc(c(c1)C)Cl)(O)O.CN=C=O
Canonical SMILES:
OB(c1ccc(c(c1)C)Cl)O.O=C=NC
InChI:
InChI=1S/C7H8BClO2.C2H3NO/c1-5-4-6(8(10)11)2-3-7(5)9;1-3-2-4/h2-4,10-11H,1H3;1H3
InChIKey:
ZMDJRYMYZQUOME-UHFFFAOYSA-N

Cite this record

CBID:298177 http://www.chembase.cn/molecule-298177.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(4-chloro-3-methylphenyl)boronic acid; isocyanatomethane
IUPAC Traditional name
4-chloro-3-methylphenylboronic acid methyl isocyanate
Synonyms
4-Chloro-3-(dimethylaminocarbonyl)phenylboronic acid
N,N-Dimethyl 5-borono-2-chlorobenzamide
4-Chloro-3-(dimethylcarbamoyl)benzeneboronic acid
4-氯-3-(二甲基氨甲酰基)苯硼酸
CAS Number
871332-76-2
MDL Number
MFCD07783868
PubChem SID
180683708
PubChem CID
73995375

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Alfa Aesar
H52519 external link Add to cart Please log in.
Data Source Data ID
PubChem 73995375 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.749236  H Acceptors
H Donor LogD (pH = 5.5) 2.6247568 
LogD (pH = 7.4) 2.6060903  Log P 2.625 
Molar Refractivity 40.4495 cm3 Polarizability 17.178318 Å3
Polar Surface Area 40.46 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
164-166°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
98% 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