(4-Chlorophenyl)boronic acid structure
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Common Name | (4-Chlorophenyl)boronic acid | ||
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CAS Number | 1679-18-1 | Molecular Weight | 156.375 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 295.4±42.0 °C at 760 mmHg | |
Molecular Formula | C6H6BClO2 | Melting Point | 284-289 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 132.4±27.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 4-Chlorophenylboronic acid |
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Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
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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 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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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 |
Precursor 9 | |
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DownStream 10 | |
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. |
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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... |
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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... |
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)- |