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Merck
CN

280097

3-溴碘苯

98%

别名:

1-Bromo-3-iodobenzene, 1-Iodo-3-bromobenzene, 3-Bromo-1-iodobenzene, 3-Bromophenyl iodide, 3-Iodo-1-bromobenzene, 3-Iodobromobenzene, 3-Iodophenyl bromide, m-Bromoiodobenzene

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关于此项目

线性分子式:
BrC6H4I
化学文摘社编号:
分子量:
282.90
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-703-9
MDL number:
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产品名称

3-溴碘苯, 98%

InChI key

CTPUUDQIXKUAMO-UHFFFAOYSA-N

InChI

1S/C6H4BrI/c7-5-2-1-3-6(8)4-5/h1-4H

SMILES string

Brc1cccc(I)c1

assay

98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.66 (lit.)

bp

120 °C/18 mmHg (lit.)

mp

−9.3-−9 °C (lit.)

density

2.219 g/mL at 25 °C (lit.)

functional group

bromo
iodo

Quality Level

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Application

3-Bromoiodobenzene has been used in the preparation of:
  • 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene
  • 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
  • oxygen-tethered 1,6-enynes

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Alexandre Pradal et al.
Beilstein journal of organic chemistry, 7, 1021-1029 (2011-09-15)
A comprehensive study on the asymmetric gold-catalyzed cycloisomerization reaction of heteroatom tethered 1,6-enynes is described. The cycloisomerization reactions were conducted in the presence of the chiral cationic Au(I) catalyst consisting of (R)-4-MeO-3,5-(t-Bu)(2)-MeOBIPHEP-(AuCl)(2) complex and silver salts (AgOTf or AgNTf(2)) in
Efficient access to perfluoroalkylated aryl compounds by Heck reaction.
Darses S, et al.
European Journal of Organic Chemistry, 2001(6), 1121-1128 (2001)
Junpei Miyake et al.
Science advances, 3(10), eaao0476-eaao0476 (2017-10-28)
Proton exchange membrane fuel cells (PEMFCs) are promising devices for clean power generation in automotive, stationary, and portable applications. Perfluorosulfonic acid (PFSA) ionomers (for example, Nafion) have been the benchmark PEMs; however, several problems, including high gas permeability, low thermal

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