145610
3-(溴甲基)苯甲腈
95%
别名:
α-溴间甲基苯甲腈, 3-氰基溴苄
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关于此项目
线性分子式:
BrCH2C6H4CN
化学文摘社编号:
分子量:
196.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
248-890-1
Beilstein/REAXYS Number:
742356
MDL number:
Assay:
95%
产品名称
3-(溴甲基)苯甲腈, 95%
InChI key
CVKOOKPNCVYHNY-UHFFFAOYSA-N
InChI
1S/C8H6BrN/c9-5-7-2-1-3-8(4-7)6-10/h1-4H,5H2
SMILES string
BrCc1cccc(c1)C#N
assay
95%
mp
93-96 °C
functional group
bromo
nitrile
Quality Level
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Application
3-(Bromomethyl)benzonitrile was used in the synthesis of 3-(bromomethyl)benzaldehyde.
General description
3-(Bromomethyl)benzonitrile undergoes Suzuki cross-coupling reaction with bis(pinacolato)diboron.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Synthesis of benzylic boronates via palladium-catalyzed cross-coupling reaction of bis (pinacolato) diboron with benzylic halides.
Giroux A.
Tetrahedron Letters, 44(2), 233-235 (2003)
Lydia C Gilday et al.
Dalton transactions (Cambridge, England : 2003), 41(23), 7092-7097 (2012-05-09)
Triazole and triazolium groups have been integrated into a zinc(II) metalloporphyrin-based structural framework to produce two porphyrin-cages for anion sensing applications. UV/visible spectroscopic titration investigations reveal both host systems exhibit strong anion binding affinities, with the positively-charged triazolium-porphyrin cage capable
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