302384
2,4,4,6-四溴-2,5-环己二烯酮
90%
别名:
TBCO
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关于此项目
经验公式（希尔记法）:
C6H2Br4O
化学文摘社编号:
分子量:
409.70
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
90%
表单
solid
官能团
bromo
ketone
储存温度
2-8°C
SMILES字符串
BrC1=CC(Br)(Br)C=C(Br)C1=O
InChI
1S/C6H2Br4O/c7-3-1-6(9,10)2-4(8)5(3)11/h1-2H
InChI key
NJQJGRGGIUNVAB-UHFFFAOYSA-N
一般描述
2,4,4,6-四溴-2,5-环己二烯酮与4-（氨基甲基）哌啶可形成固体电荷转移分子配合物，并且其光谱特征已有研究。
应用
使用2,4,4,6-四溴-2,5-环己二烯酮作为催化剂，使亚砜与1,3-二噻烷有效脱氧形成相应的硫化物。 它还被用作将醇转化为叠氮化物的试剂。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Darren Van Essen et al.
Chemosphere, 266, 129195-129195 (2020-12-15)
Brominated flame retardants (BFRs) can enter aquatic environments where they can have adverse effects on organisms. The BFR, 1,2,5,6-Tetrabromocyclooctane (TBCO), has been introduced as a potential replacement for the major use BRF, Hexabromocyclododecane (HBCD). However, little is known about effects
Adel Mostafa et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 118, 1012-1019 (2013-11-05)
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 the π-acceptors 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TBCHD) and 7,7,8,8-tetracyanoquinodimethane (TCNQ) have been studied in chloroform
Giulia Simonetti et al.
International journal of environmental research and public health, 17(11) (2020-05-31)
The occurrence of halogenated organic pollutants in indoor dust can be high due to the presence of textile, electronic devices, furniture, and building materials treated with these chemicals. In this explorative study, we focused on emerging organic pollutants, such as
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 Letters, 38(22), 3955-3958 (1997)
Nasser Iranpoor et al.
The Journal of organic chemistry, 67(9), 2826-2830 (2002-04-27)
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-bromosuccinimide (NBS), 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO), or Br(2) as the source of
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