2,4,4,6-tetrabromo-2,5-cyclohexadienone structure
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Common Name | 2,4,4,6-tetrabromo-2,5-cyclohexadienone | ||
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CAS Number | 20244-61-5 | Molecular Weight | 409.69500 | |
Density | 2.897 g/cm3 | Boiling Point | 365.8ºC at 760 mmHg | |
Molecular Formula | C6H2Br4O | Melting Point | 120-127 °C | |
MSDS | Chinese USA | Flash Point | 136ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2,4,4,6-tetrabromocyclohexa-2,5-dien-1-one |
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Synonym | More Synonyms |
Density | 2.897 g/cm3 |
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Boiling Point | 365.8ºC at 760 mmHg |
Melting Point | 120-127 °C |
Molecular Formula | C6H2Br4O |
Molecular Weight | 409.69500 |
Flash Point | 136ºC |
Exact Mass | 405.68400 |
PSA | 17.07000 |
LogP | 3.61280 |
Vapour Pressure | 1.53E-05mmHg at 25°C |
Index of Refraction | 1.757 |
Storage condition | 0-6°C |
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 | 2914700090 |
Precursor 10 | |
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DownStream 9 | |
HS Code | 2914700090 |
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Summary | HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0% |
A new approach to the reduction of sulfoxides to sulfides with 1,3-dithiane in the presence of electrophilic bromine as catalyst.
J. Org. Chem. 67(9) , 2826-30, (2002) A new, mild, and novel method is described for the efficient deoxygenation of sulfoxides to their corresponding sulfides with 1,3-dithiane at room temperature in the presence of catalytic amounts of N... |
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Spectrophotometric and thermal studies on the charge--transfer complexes of 4-(aminomethyl) piperidine as donor with σ- and π-electron acceptors.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 118 , 1012-9, (2014) The spectroscopic characteristics of the solid charge-transfer molecular complexes (CT) formed in the reaction of the electron donor 4-(aminomethyl) piperidine (4AMP) with the σ-acceptor iodine and th... |
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An efficient method for converting alcohols to azides with 2, 4, 4, 6-tetrabromo-2, 5-cyclohexadienone/PPh3 /Zn (N3)2· 2Py. Saito A, et al.
Tetrahedron Lett. 38(22) , 3955-58, (1997)
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2,4,4,6-tetrabromo-2,5-cyclohexadieneone |
2,4,4,6-Tetrabromocyclohexa-2,5-dienone |
EINECS 243-638-7 |
2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one |
MFCD00001589 |
2,4,4,6-TetrabroMo-2,5-cyclohexadienone |
2,3-DIFLUOROPHENYLGLYCINE |