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About This Item
线性分子式:
BrCH2C6H4CN
CAS号:
分子量:
196.04
Beilstein:
742356
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
品質等級
化驗
95%
mp
93-96 °C
官能基
bromo
nitrile
SMILES 字串
BrCc1cccc(c1)C#N
InChI
1S/C8H6BrN/c9-5-7-2-1-3-8(4-7)6-10/h1-4H,5H2
InChI 密鑰
CVKOOKPNCVYHNY-UHFFFAOYSA-N
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一般說明
3-(Bromomethyl)benzonitrile undergoes Suzuki cross-coupling reaction with bis(pinacolato)diboron.
應用
3-(Bromomethyl)benzonitrile was used in the synthesis of 3-(bromomethyl)benzaldehyde.
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
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)
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