5-Bromo-2-furaldehyde structure
|
Common Name | 5-Bromo-2-furaldehyde | ||
---|---|---|---|---|
CAS Number | 1899-24-7 | Molecular Weight | 174.980 | |
Density | 1.7±0.1 g/cm3 | Boiling Point | 222.9±20.0 °C at 760 mmHg | |
Molecular Formula | C5H3BrO2 | Melting Point | 82-85 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 88.6±21.8 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 5-bromofuran-2-carbaldehyde |
---|---|
Synonym | More Synonyms |
Density | 1.7±0.1 g/cm3 |
---|---|
Boiling Point | 222.9±20.0 °C at 760 mmHg |
Melting Point | 82-85 °C(lit.) |
Molecular Formula | C5H3BrO2 |
Molecular Weight | 174.980 |
Flash Point | 88.6±21.8 °C |
Exact Mass | 173.931641 |
PSA | 30.21000 |
LogP | 1.77 |
Vapour Pressure | 0.1±0.4 mmHg at 25°C |
Index of Refraction | 1.573 |
Storage condition | Refrigerator |
Stability | Stable. Incompatible with strong oxidizing agents. |
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H302-H312-H315-H319-H332-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R20/21/22;R36/37/38 |
Safety Phrases | S26-S36-S36/37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2932190090 |
Precursor 9 | |
---|---|
DownStream 10 | |
HS Code | 2932190090 |
---|---|
Summary | 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
5-Substituted-2-furaldehydes: a synthetic protocol utilizing an organozinc route.
J. Org. Chem. 78(5) , 1984-93, (2013) Facile synthetic routes for the preparation of a wide range of 5-substituted 2-furaldehydes have been revealed. They were accomplished through either Pd-catalyzed cross-coupling reaction of various ar... |
|
From furans to anilines: toward one-pot two-step amination/diels-alder sequences.
J. Org. Chem. 73(6) , 2191-7, (2008) Selective metal-free amination and Diels-Alder reactions are described in the furan series, leading to polysubstituted anilines or to stable oxabicyclic adducts in high yield. Interestingly, anilines ... |
|
Efficient coupling of heteroaryl bromides with arylboronic acids in the presence of a palladium-tetraphosphine catalyst. Feuerstein M, et al.
Tetrahedron Lett. 42(23) , 5659-62, (2001)
|
5-Bromofurfural |
5-bromofuran-2-carbaldehyde |
5-Bromofurancarboxaldehyde |
5-bromo-2-furancarboxaldehyde |
5-bromofuran-2-yl carbaldehyde |
2-Furaldehyde, 5-bromo- |
2-Furancarboxaldehyde, 5-bromo- |
5'-bromo-furan-2'-carboxaldehyde |
5-Bromo-2-furaldehyde |
5-bromo-furfurol |
5-bromo-2-furfural |
2-Furancarboxaldehyde,5-bromo |
MFCD00159501 |