Cyclopropylboronic acid structure
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Common Name | Cyclopropylboronic acid | ||
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CAS Number | 411235-57-9 | Molecular Weight | 85.90 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 205.1±23.0 °C at 760 mmHg | |
Molecular Formula | C3H7BO2 | Melting Point | 90-95 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 77.9±22.6 °C | |
Symbol |
GHS05, GHS07, GHS08 |
Signal Word | Danger |
Use of Cyclopropylboronic acidCyclopropaneboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | Cyclopropylboronic acid |
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Synonym | More Synonyms |
Description | Cyclopropaneboronic 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 | 205.1±23.0 °C at 760 mmHg |
Melting Point | 90-95 °C(lit.) |
Molecular Formula | C3H7BO2 |
Molecular Weight | 85.90 |
Flash Point | 77.9±22.6 °C |
Exact Mass | 86.053909 |
PSA | 40.46000 |
LogP | 0.20 |
Vapour Pressure | 0.1±0.9 mmHg at 25°C |
Index of Refraction | 1.443 |
Storage condition | Store below -20 |
Symbol |
GHS05, GHS07, GHS08 |
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Signal Word | Danger |
Hazard Statements | H302-H318-H360FD |
Precautionary Statements | P201-P280-P305 + P351 + P338-P308 + P313 |
Hazard Codes | Xn:Harmful |
Risk Phrases | R22 |
Safety Phrases | S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2942000000 |
Precursor 5 | |
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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% |
Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids.
Org. Lett. 13 , 6114-6117, (2011) The decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd(2)(dba)(3) and DPEphos, achieving aryl o-aminobenzoates with yields rang... |
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Palladium-catalyzed alkylation of sp2 and sp3 C-H bonds with methylboroxine and alkylboronic acids: two distinct C-H activation pathways.
J. Am. Chem. Soc. 128 , 12634, (2006) Palladium-catalyzed alkylations of sp2 and sp3 C-H bonds with either methylboroxine or alkylboronic acids were developed. Ag2O or AgCO3 is used as a crucial oxidant and promoter for the transmetalatio... |
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Copper-mediated N-cyclopropylation of azoles, amides, and sulfonamides by cyclopropylboronic acid.
J. Org. Chem. 73 , 6441, (2008) Reaction of azoles, amides, and sulfonamides in dichloroethane with readily available cyclopropylboronic acid in the presence of copper acetate and sodium carbonate afforded the N-cyclopropyl derivati... |
MFCD04038750 |
acide cyclopropylboronique |
Cyclopropyl Boronic Acid |
Boronic acid, B-cyclopropyl- |
Cyclopropylboronic acid |
Cyclopropaneboronic acid |
cyclopropyl boronic |