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4-Chlorophenylmagnesium iodide is an organomagnesium compound with the chemical formula C6H4ClMgI. It is a colorless to pale yellow solid that is highly reactive and sensitive to air and moisture. 4-chlorophenylmagnesium iodide is an important intermediate in organic synthesis, particularly in the preparation of various 4-chlorophenyl-containing compounds. It is typically synthesized by reacting 4-chlorobromobenzene with magnesium metal in anhydrous ether or tetrahydrofuran. Due to its high reactivity, 4-chlorophenylmagnesium iodide is often used in Grignard reactions to form carbon-carbon bonds, and it can also be employed in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Handling of 4-chlorophenylmagnesium iodide requires strict exclusion of air and moisture, and it is commonly stored under an inert atmosphere or in a sealed container.

7270-47-5

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7270-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7270-47-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7270-47:
(6*7)+(5*2)+(4*7)+(3*0)+(2*4)+(1*7)=95
95 % 10 = 5
So 7270-47-5 is a valid CAS Registry Number.

7270-47-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chlorophenylmagnesium iodide

1.2 Other means of identification

Product number -
Other names 4-Chlor-phenylmagnesiumjodid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7270-47-5 SDS

7270-47-5Upstream product

7270-47-5Relevant academic research and scientific papers

An N-Fluorinated Imide for Practical Catalytic Imidations

Oe, Yuno,Yoshida, Ryuhei,Tanaka, Airi,Adachi, Akiya,Ishibashi, Yuichiro,Okazoe, Takashi,Aikawa, Kohsuke,Hashimoto, Takuya

supporting information, p. 2107 - 2113 (2022/02/10)

Catalytic imidation using NFSI as the nitrogen source has become an emerging tool for oxidative carbon-nitrogen bond formation. However, the less than ideal benzenesulfonimide moiety is incorporated into products, severely detracting its synthetic value.

Efficient C(sp3)-H bond functionalization of isochroman by azadol catalysis

Muramatsu, Wataru,Nakano, Kimihiro

supporting information, p. 1549 - 1552 (2015/03/30)

A novel organocatalytic C(sp3)-H bond functionalization of isochroman under practical conditions has been developed. In the presence of 5.0 mol % of AZADOL, the catalysis proceeded successfully with a broad range of substrates and nucleophiles in excellent yields.

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