2,4,4,6-tetrabromo-2,5-cyclohexadienone

Modify Date: 2024-01-02 10:56:00

2,4,4,6-tetrabromo-2,5-cyclohexadienone Structure
2,4,4,6-tetrabromo-2,5-cyclohexadienone structure
Common Name 2,4,4,6-tetrabromo-2,5-cyclohexadienone
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
GHS07
Signal Word Warning

 Names

Name 2,4,4,6-tetrabromocyclohexa-2,5-dien-1-one
Synonym More Synonyms

 Chemical & Physical Properties

Density 2.897 g/cm3
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

 Safety Information

Symbol GHS07
GHS07
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

 Synthetic Route

 Customs

HS Code 2914700090
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%

 Articles3

More Articles
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...

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...

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)

 Synonyms

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
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