p-Boronobenzoic acid structure
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Common Name | p-Boronobenzoic acid | ||
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CAS Number | 14047-29-1 | Molecular Weight | 165.94 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 406.4±47.0 °C at 760 mmHg | |
Molecular Formula | C7H7BO4 | Melting Point | 220 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | 199.6±29.3 °C |
Use of p-Boronobenzoic acid4-Boronobenzoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 4-Carboxyphenylboronic acid |
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Synonym | More Synonyms |
Description | 4-Boronobenzoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 406.4±47.0 °C at 760 mmHg |
Melting Point | 220 °C (dec.)(lit.) |
Molecular Formula | C7H7BO4 |
Molecular Weight | 165.94 |
Flash Point | 199.6±29.3 °C |
Exact Mass | 166.043747 |
PSA | 77.76000 |
LogP | 1.27 |
Vapour Pressure | 0.0±1.0 mmHg at 25°C |
Index of Refraction | 1.585 |
Storage condition | 0-6°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 2 |
RTECS | CY8925000 |
Precursor 10 | |
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DownStream 10 | |
Highly efficient aerobic oxidative hydroxylation of arylboronic acids: photoredox catalysis using visible light.
Angew. Chem. Int. Ed. Engl. 3rd ed., 51 , 784-788, (2012)
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A new access to 3-substituted-1(2H)-isoquinolone by tandem palladium-catalyzed intramolecular aminocarbonylation annulation.
Org. Biomol. Chem. 13th ed., 10 , 2683-2691, (2012) An original tribromide derivative based, palladium-catalyzed synthesis of 3-substituted-1(2H)-isoquinolone is described based on a regioselective Suzuki-Miyaura C-C coupling on o-halo-(2,2-dihalovinyl... |
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Synthesis of new trisulfonated calix[4]arenes functionalized at the upper rim, and their complexation with the trimethyllysine epigenetic mark.
Org. Lett. 6th ed., 14 , 1512-1515, (2012) A synthetic route to produce a new family of trisulfonated calix[4]arenes bearing a single group, selectively introduced, that lines the binding pocket is reported. Ten examples, including new sulfona... |
4-(Dihydroxyboryl)benzoic acid |
Benzoic acid, 4-borono- |
4-Carboxybenzeneboronic Acid |
4-Boronobenzoic acid |
MFCD00151801 |
4-Carboxyphenylboronic acid |
p-Carboxybenzeneboronic acid |
p-Boronobenzoic acid |
4-(dihydroxyboranyl)benzoic acid |