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Merck
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文件

335762

Sigma-Aldrich

1-溴-4-丁基苯

97%

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About This Item

线性分子式:
CH3(CH2)3C6H4Br
CAS号:
41492-05-1
分子量:
213.11
MDL號碼:
MFCD00040934
分類程式碼代碼:
12352100
PubChem物質ID:
24860344
NACRES:
NA.22

化驗

97%

形狀

liquid

折射率

n20/D 1.53 (lit.)

密度

1.208 g/mL at 25 °C (lit.)

SMILES 字串

CCCCc1ccc(Br)cc1

InChI

1S/C10H13Br/c1-2-3-4-9-5-7-10(11)8-6-9/h5-8H,2-4H2,1H3

InChI 密鑰

BRGVKVZXDWGJBX-UHFFFAOYSA-N

一般說明

Phosphite or phosphine oxide ligand catalyzed Suzuki-Miyaura reaction of 2-pyridyl boron derivatives with 1-bromo-4-butylbenzene has been reported.

應用

1-Bromo-4-butylbenzene was used in the preparation of:
  • 4-(4-butylphenyl)-2-methylbut-3-yn-2-ol
  • teraaza- and hexaazacyclophane
  • 4-butyltriphenylamine, monomer required for the preparation of poly(4-butyltriphenylamine)

象形圖

CorrosionEnvironment
GHS05,GHS09

訊號詞

Danger

危險聲明

H315,H318,H410

危險分類

Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

226.4 °F - closed cup

閃點（°C）

108 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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双（频哪醇合）二硼 99%

Sigma-Aldrich

473294

双（频哪醇合）二硼

[Pd2(dba)3] x dba Umicore

Sigma-Aldrich

683345

[Pd2(dba)3] x dba

A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles.
Kelvin L Billingsley et al.
Angewandte Chemie (International ed. in English), 47(25), 4695-4698 (2008-05-21)
Irena Kulszewicz-Bajer et al.
Physical chemistry chemical physics : PCCP, 11(9), 1362-1368 (2009-02-19)
Teraaza- and hexaazacyclophanes have been synthesized via a one-step palladium catalyzed amination reaction. The chemical oxidation of cyclophanes leads to the formation of radical cations, the presence of which was manifested by the appearance of new bands in UV-Vis-NIR and
Synthesis and characterization of the multi-photon absorption and excited-state properties of a neat liquid 4-propyl 4'-butyl diphenyl acetylene
Khoo LC, et al.
Journal of Materials Chemistry, 19(40), 7525-7525 (2009)
Preparation of poly (4-butyltriphenylamine) particles by chemical oxidative dispersion polymerization.
Fujioka M, et al.
Coll. Polymer Sci., 286(3), 313-318 (2008)

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