B82006
2-溴甲苯
99%
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关于此项目
线性分子式:
CH3C6H4Br
化学文摘社编号:
分子量:
171.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-421-7
Beilstein/REAXYS Number:
1904176
MDL number:
产品名称
2-溴甲苯, 99%
InChI key
QSSXJPIWXQTSIX-UHFFFAOYSA-N
InChI
1S/C7H7Br/c1-6-4-2-3-5-7(6)8/h2-5H,1H3
SMILES string
Cc1ccccc1Br
assay
99%
form
liquid
refractive index
n20/D 1.555 (lit.)
bp
58-60 °C/10 mmHg (lit.)
mp
−27 °C (lit.)
density
1.422 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
2-溴甲苯可用于合成（±）-异辛烯。
General description
2-溴甲苯是一种富含电子的杂芳基溴。 Tedicip（顺式，顺式，顺式-1,2,3,4-四（二苯基膦甲基）环戊烷）-钯配合物催化带有环烯烃（环十二烯）的2-溴甲苯与线性烯烃（DEC-1-烯，烯丙基苯）的Heck反应已有研究。 2-溴苯在50-4000cm-1处的振动拉曼红外光谱已有研究。 由Tedicyp-钯络合物催化的2-溴苯与苯硼酸的Suzuki交叉偶联反应已有研究。 使用负载在氧化铝基氧化物上的钯纳米颗粒作为催化剂，2-溴甲苯与苯基硼酸的Suzuki偶联反应已有报道。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F
flash_point_c
79 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Tetraphosphine/palladium-catalysed Suzuki cross-coupling with sterically hindered aryl bromides and arylboronic acids.
Feuerstein M, et al.
Tetrahedron Letters, 42(38), 6667-6670 (2001)
Heck reaction of aryl halides with linear or cyclic alkenes catalysed by a tetraphosphine/palladium catalyst.
Berthiol F, et al.
Tetrahedron Letters, 44(6), 1221-1225 (2003)
Synthetic studies on arene-olefin cycloadditions. ii. total synthesis of (?)-isocomene.
Wender PA and Geoffrey BD.
Tetrahedron, 37(25), 4445-4450 (1981)
Palladium nanoparticles supported on alumina-based oxides as heterogeneous catalysts of the Suzuki-Miyaura reaction.
Gniewek A, et al.
J. Catal., 254(1), 121-130 (2008)
Sven Herbers et al.
Physical chemistry chemical physics : PCCP, 22(20), 11490-11497 (2020-05-12)
The internal rotation of methyl groups and nuclear quadrupole moments of the halogens Cl, Br, I in o-halotoluenes cause complex spectral fine and hyperfine structures in rotational spectra arising from angular momentum coupling. Building on the existing data regarding o-fluorotoluene
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