4-Tolylboronic acid structure
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Common Name | 4-Tolylboronic acid | ||
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CAS Number | 5720-05-8 | Molecular Weight | 135.956 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 275.2±33.0 °C at 760 mmHg | |
Molecular Formula | C7H9BO2 | Melting Point | 256-263 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 120.2±25.4 °C |
Use of 4-Tolylboronic acid4-Tolueneboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 4-Methylphenylboronic Acid |
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Synonym | More Synonyms |
Description | 4-Tolueneboronic 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 | 1.1±0.1 g/cm3 |
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Boiling Point | 275.2±33.0 °C at 760 mmHg |
Melting Point | 256-263 °C(lit.) |
Molecular Formula | C7H9BO2 |
Molecular Weight | 135.956 |
Flash Point | 120.2±25.4 °C |
Exact Mass | 136.069565 |
PSA | 12.03000 |
LogP | 2.05 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.528 |
Storage condition | 0-6°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | XS7400000 |
HS Code | 2931900090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2931900090 |
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Summary | 2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0% |
Carbonic anhydrase inhibitors. Inhibition of the fungal beta-carbonic anhydrases from Candida albicans and Cryptococcus neoformans with boronic acids.
Bioorg. Med. Chem. Lett. 19 , 2642-5, (2009) Inhibition of the beta-carbonic anhydrases (CAs, EC 4.2.1.1) from the pathogenic fungi Cryptococcus neoformans (Can2) and Candida albicans (Nce103) with a series of aromatic, arylalkenyl- and arylalky... |
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Direct palladium(II)-catalyzed synthesis of arylamidines from aryltrifluoroborates.
Org. Lett. 9th ed., 14 , 2394-2397, (2012) A fast and convenient synthesis of arylamidines starting from readily available potassium aryltrifluoroborates and cyanamides is reported. The coupling was achieved by Pd(II)-catalysis in a one step 2... |
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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... |
(R)-N-methyl-1-phenylethanamine |
(4-Methylphenyl)boronic acid |
((1R)-1-phenylethyl)methylamine |
Boronic acid, B-(4-methylphenyl)- |
Benzenemethanamine, N,α-dimethyl-, (αR)- |
4-Tolylboronic acid |
MFCD00039138 |
4-Methylphenylboronic acid |
(1R)-N-Methyl-1-phenylethanamine |
(R)-N-Methyl-α-phenylethylamine |
EINECS 202-766-3 |