2-Bromo-1H-isoindole-1,3(2H)-dione structure
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Common Name | 2-Bromo-1H-isoindole-1,3(2H)-dione | ||
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CAS Number | 2439-85-2 | Molecular Weight | 226.027 | |
Density | 1.9±0.1 g/cm3 | Boiling Point | 332.3±25.0 °C at 760 mmHg | |
Molecular Formula | C8H4BrNO2 | Melting Point | 194-198 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 154.8±23.2 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2-bromoisoindole-1,3-dione |
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Synonym | More Synonyms |
Density | 1.9±0.1 g/cm3 |
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Boiling Point | 332.3±25.0 °C at 760 mmHg |
Melting Point | 194-198 °C(lit.) |
Molecular Formula | C8H4BrNO2 |
Molecular Weight | 226.027 |
Flash Point | 154.8±23.2 °C |
Exact Mass | 224.942535 |
PSA | 37.38000 |
LogP | 1.72 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.705 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2925190090 |
Precursor 6 | |
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DownStream 9 | |
HS Code | 2925190090 |
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Summary | 2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
Enantioselective synthesis of multisubstituted biaryl skeleton by chiral phosphoric acid catalyzed desymmetrization/kinetic resolution sequence.
J. Am. Chem. Soc. 135(10) , 3964-70, (2013) Described herein is the enantioselective synthesis of multisubstituted biaryl derivatives by chiral phosphoric acid catalyzed asymmetric bromination. Two asymmetric reactions (desymmetrization and kin... |
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Titrimetric determination of acetylenic hyponotics using organic brominating agents.
Pharm. Weekbl. Sci. 10(2) , 90-2, (1988) A titrimetric method is described for the determination of three acetylenic hypnotics, namely ethchlorvynol, ethinamate, and methylpentynol carbamate, in bulk and in dosage forms. The method involves ... |
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N-bromoimide/DBU combination as a new strategy for intermolecular allylic amination.
Org. Lett. 15(20) , 5186-9, (2013) Allylic amination reactions of alkenes, with an NBP (N-bromophthalimide) or NBS (N-bromosuccinimide)/DBU combination, were developed, in which both internal and external nitrogen nucleophiles can be i... |
N-Bromophthalimide |
N-bromoisoindole-1,3-dione |
2-Bromoisoindoline-1,3-dione |
EINECS 219-467-9 |
MFCD00005888 |
1H-Isoindole-1,3(2H)-dione, 2-bromo- |
2-Bromo-1H-isoindole-1,3(2H)-dione |