(4-Chlorophenyl)boronic acid

Names

[ Name ]:
(4-Chlorophenyl)boronic acid

[Synonym ]:
4-Chlorophenylboranic acid
p-chlorophenylboronic aci
para-chlorophenylboronic acid
(4-Chlorophenyl)boronic acid
para-chlorobenzene boronic acid
4-CHLOROPHENYLBORNIC ACID
p-chloro-benzeneboronicaci
MFCD00039137
boronicacid,p-chlorophenyl
4-Chlorophenylboronic acid
EINECS 216-845-5
4-chlorobenzeneboronic acid
4-Chloro phenyl boronic acid
p-chlorophenylboronic acid
p-chlorobenzeneboronic acid
RARECHEM AH PB 0178
Boronic acid, B-(4-chlorophenyl)-

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
295.4±42.0 °C at 760 mmHg

[ Melting Point ]:
284-289 °C(lit.)

[ Molecular Formula ]:
C₆H₆BClO₂

[ Molecular Weight ]:
156.375

[ Flash Point ]:
132.4±27.9 °C

[ Exact Mass ]:
156.014938

[ PSA ]:
40.46000

[ LogP ]:
2.18

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.558

[ Storage condition ]:
Refrigerator (+4°C)

[ Water Solubility ]:
2.5 g/100 mL

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: CY8950000

CHEMICAL NAME :: Benzeneboronic acid, p-chloro-

CAS REGISTRY NUMBER :: 1679-18-1

BEILSTEIN REFERENCE NO. :: 2936346

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C6-H6-B-Cl-O2

MOLECULAR WEIGHT :: 156.38

WISWESSER LINE NOTATION :: QBQR DG

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 180 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#00061

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S36-S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
CY8950000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Cationic Pd(II)-catalyzed highly enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes with arylboronic acids.

Org. Lett. 7th ed., 14 , 1756-1759, (2012)

Cationic Pd(II)-catalyzed enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes was developed without the necessity of a redox system.

Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.

Org. Lett. 7th ed., 14 , 1930-1933, (2012)

A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combin...

Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.

Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)

A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction an...