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主要文件

206555

Sigma-Aldrich

4-碘甲苯

99%

别名:

4-碘代甲苯

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1 EA
¥2,030.19

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预计发货时间2025年5月13日详情


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1 EA
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About This Item

线性分子式:
CH3C6H4I
CAS号:
分子量:
218.03
Beilstein:
1903637
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

¥2,030.19


预计发货时间2025年5月13日详情


获取大包装报价

质量水平

方案

99%

表单

solid

沸点

211.5 °C (lit.)

mp

33-35 °C (lit.)

官能团

iodo

SMILES字符串

Cc1ccc(I)cc1

InChI

1S/C7H7I/c1-6-2-4-7(8)5-3-6/h2-5H,1H3

InChI key

UDHAWRUAECEBHC-UHFFFAOYSA-N

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此商品
ECM001SRP3186ECM104
Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

shipped in

wet ice

shipped in

ambient

shipped in

wet ice

shipped in

wet ice

NCBI accession no.

NM_002026.2, NM_212474.1, NM_212476.1, NM_212482.1, NM_054034.2, NM_212478.1, NM_212475.1

NCBI accession no.

NM_212482.4

NCBI accession no.

NM_000638.4

NCBI accession no.

NM_000088.3

UniProt accession no.

P02751

UniProt accession no.

P02751

UniProt accession no.

P04004

UniProt accession no.

P02452

species reactivity

human

species reactivity

-

species reactivity

-

species reactivity

human

一般描述

4-碘甲苯在负载钯的 (Ni,Mg) 3 Si 2 O 5 (OH) 4 固溶体纳米管催化下与苯硼酸发生 Suzuki-Miyaura 偶联反应 [1]。对钴催化 4-碘甲苯与硫酚和硫醇的偶联反应进行了研究 [2]。研究了钯/铜催化的 4-碘甲苯与苯乙炔的薗头交叉偶联反应[3]

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

194.0 °F - closed cup

闪点(°C)

90 °C - closed cup

个人防护装备

Eyeshields, Gloves, type N95 (US)


  • 历史批次信息供参考:

    分析证书(COA)

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    Wancheng Zhu et al.
    Inorganic chemistry, 51(11), 6020-6031 (2012-05-16)
    (Ni(1-x),Mg(x))(3)Si(2)O(5)(OH)(4) solid-solution nanotubes (NTs) with tunable compositions were hydrothermally synthesized by altering the molar ratio of Mg(2+) to Ni(2+). The as-synthesized NTs were loaded with sub-0.06 wt % palladium (Pd; ∼0.045 wt %) for Suzuki-Miyaura (SM) coupling reactions between iodobenzene
    Takashi Mino et al.
    The Journal of organic chemistry, 71(25), 9499-9502 (2006-12-02)
    Palladium/copper-catalyzed Sonogashira cross-coupling reaction of aryl halides with a variety of terminal alkynes under amine-free conditions in dimethylformamide (DMF) at 80 degrees C gave internal arylated alkynes using PdCl2(MeCN)2 with phosphine-free hydrazone 2a as a ligand and CuI as the
    Ying-Chieh Wong et al.
    Organic letters, 8(24), 5613-5616 (2006-11-17)
    A new cobalt-catalyzed coupling of aryl halides with thiophenols and alkanethiols is reported. A variety of aryl sulfides can be prepared in excellent yields under mild reaction conditions using 1-2 mol % of CoI2(dppe) and Zn. This new cobalt-catalyzed coupling
    V Kolaříková et al.
    Dalton transactions (Cambridge, England : 2003), 44(45), 19663-19673 (2015-09-17)
    Using three different approaches, racemic 1-(perfluoroalkyl)ethylamines were synthesized from perfluoroalkyl iodides or perfluoroalkanoic acids, and further transformed to the corresponding N,N'-disubstituted ethane-1,2-diimines and ethane-1,2-diamines as mixtures of diastereoisomers. Their cyclization afforded imidazolium or dihydroimidazolium salts, which led to silver or
    Zengyan Wei et al.
    Nature communications, 5, 3870-3870 (2014-05-16)
    The shape-controlled synthesis of nanoparticles was established in single-phase solutions by controlling growth directions of crystalline facets on seed nanocrystals kinetically; however, it was difficult to rationally predict and design nanoparticle shapes. Here we introduce a methodology to fabricate nanoparticles

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