styrylboronic acid structure
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Common Name | styrylboronic acid | ||
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CAS Number | 6783-05-7 | Molecular Weight | 147.967 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 315.9±35.0 °C at 760 mmHg | |
Molecular Formula | C8H9BO2 | Melting Point | 146-156 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 144.9±25.9 °C |
Name | e-phenylethenylboronic acid |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 315.9±35.0 °C at 760 mmHg |
Melting Point | 146-156 °C(lit.) |
Molecular Formula | C8H9BO2 |
Molecular Weight | 147.967 |
Flash Point | 144.9±25.9 °C |
Exact Mass | 148.069565 |
PSA | 40.46000 |
LogP | 2.57 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.587 |
Storage condition | 0-6°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Risk Phrases | R36/37/38 |
Safety Phrases | S37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2931900090 |
~51% styrylboronic acid CAS#:6783-05-7 |
Literature: Tetrahedron, , vol. 67, # 3 p. 576 - 583 |
~97% styrylboronic acid CAS#:6783-05-7 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 15, # 11 p. 2803 - 2807 |
~90% styrylboronic acid CAS#:6783-05-7 |
Literature: Bioorganic and Medicinal Chemistry, , vol. 12, # 15 p. 4285 - 4299 |
~64% styrylboronic acid CAS#:6783-05-7 |
Literature: Journal of Organic Chemistry, , vol. 74, # 19 p. 7364 - 7369 |
~71% styrylboronic acid CAS#:6783-05-7 |
Literature: Journal of Organometallic Chemistry, , vol. 507, # 1-2 p. 207 - 214 |
~% styrylboronic acid CAS#:6783-05-7 |
Literature: Journal of Organometallic Chemistry, , vol. 5, p. 506 - 519 |
~% styrylboronic acid CAS#:6783-05-7 |
Literature: Journal of the American Chemical Society, , vol. 97, # 19 p. 5608 - 5609 |
Precursor 7 | |
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DownStream 9 | |
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% |
Rh2(II)-catalyzed intramolecular aliphatic C-H bond amination reactions using aryl azides as the N-atom source.
J. Am. Chem. Soc. 17th ed., 134 , 7262-7265, (2012) Rhodium(II) dicarboxylate complexes were discovered to catalyze the intramolecular amination of unactivated primary, secondary, or tertiary aliphatic C-H bonds using aryl azides as the N-atom precurso... |
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Copper-mediated sequential cyanation of aryl C-B and arene C-H bonds using ammonium iodide and DMF.
J. Am. Chem. Soc. 5th ed., 134 , 2528-2531, (2012) The cyanation of aromatic boronic acids, boronate esters, and borate salts was developed under copper-mediated oxidative conditions using ammonium iodide and DMF as the source of nitrogen and carbon a... |
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Ambient temperature synthesis of high enantiopurity N-protected peptidyl ketones by peptidyl thiol ester-boronic acid cross-coupling.
J. Am. Chem. Soc. 129 , 1132, (2007) alpha-Amino acid thiol esters derived from N-protected mono-, di-, and tripeptides couple with aryl, pi-electron-rich heteroaryl, or alkenyl boronic acids in the presence of stoichiometric Cu(I) thiop... |
TRANS-B-STYRENEBORONIC ACID |
[(E)-2-Phenylvinyl]boronic acid |
trans-2-styrylboronic acid |
TRANS-PHENYLVINYLBORONIC ACID |
MFCD00963621 |
trans-styreneboronic acid |
styrylboronic acid |
trans-phenylethenyl boronic acid |
dihydroxy-(E)-styrylborane |
TRANS-2-PHENYLVINYLBORONIC ACID |
RARECHEM AH PB 0201 |
Phenylethenylboronicacid |
Boronic acid, B-[(E)-2-phenylethenyl]- |
(E)-Styreneboronic acid |