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224448

Sigma-Aldrich

苯基氯化镁 溶液

2.0 M in THF

别名:

Chlorophenylmagnesium

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About This Item

线性分子式:
C6H5MgCl
CAS号:
100-59-4
分子量:
136.86
Beilstein:
3587900
MDL號碼:
MFCD00000464
分類程式碼代碼:
12352103
PubChem物質ID:
24853438
NACRES:
NA.22

品質等級

200

反應適用性

reaction type: Grignard Reaction

濃度

2.0 M in THF

密度

~1.02 g/mL at 20 °C
1.042 g/mL at 25 °C

SMILES 字串

Cl[Mg]c1ccccc1

InChI

1S/C6H5.ClH.Mg/c1-2-4-6-5-3-1;;/h1-5H;1H;/q;;+1/p-1

InChI 密鑰

GQONLASZRVFGHI-UHFFFAOYSA-M

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相关类别

應用

苯基氯化镁 (PhMgCl) 溶液是一种常用的格氏试剂，用于合成 (-) - 苯羟基丙氨酸和 stephacidin B。它用于多种交叉偶联反应。 它也可以与氯化铝 (AlCl3) 一起在可充电镁电池中用作电解质溶液。

包裝

查看可回收的容器产品。

其他說明

25°C 以下储存可能会形成结晶镁盐。将容器移动至温暖位置，偶尔轻轻涡旋应使固体重新溶解

訊號詞

Danger

危險分類

Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

標靶器官

Respiratory system

安全危害

EUH019

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

1.4 °F - closed cup

閃點（°C）

-17 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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分析证书(COA)

Lot/Batch Number
SHBL3418
SHBM0906
SHBM0027
SHBL9403
STBJ1495

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Enantioselective synthesis of stephacidin B.
Herzon S, et al.
Journal of the American Chemical Society, 127(15), 5342-5344 (2005)
Asymmetric synthesis of pyrrolidinoindolines. Application for the practical total synthesis of (−)-phenserine
Huang A, et al.
Journal of the American Chemical Society, 126(43), 14043-14053 (2004)
Functional group tolerant Kumada- Corriu- Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: Catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents.
Vechorkin O, et al.
Journal of the American Chemical Society, 131(28), 9756-9766 (2009)
Electrolyte solutions with a wide electrochemical window for rechargeable magnesium batteries.
Mizrahi O, et al.
Journal of the Electrochemical Society, 155(2), A103-A109 (2008)
Nickel-Catalyzed Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents.
B ohm VPW, et al.
Angewandte Chemie (International Edition in English), 39(9), 1602-1604 (2000)
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Reagents for C–C Bond Formation

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

Reagents for C–C Bond Formation

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

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