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Benzoyl chloride, 4,4'-(1,2-ethenediyl)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23730-63-4

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23730-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23730-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23730-63:
(7*2)+(6*3)+(5*7)+(4*3)+(3*0)+(2*6)+(1*3)=94
94 % 10 = 4
So 23730-63-4 is a valid CAS Registry Number.

23730-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-carbonochloridoylphenyl)ethenyl]benzoyl chloride

1.2 Other means of identification

Product number -
Other names Stilben-4,4'-dicarbonsaeuredichlorid

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:23730-63-4 SDS

23730-63-4Downstream Products

23730-63-4Relevant academic research and scientific papers

Dinuclear gadolinium-containing magnetic resonance contrast agent and preparation and application thereof

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Paragraph 0039-0040; 0044-0045; 0049-0050, (2019/07/25)

The invention relates to the field of MRI (magnetic resonance imaging), in particular to a dinuclear gadolinium-containing MRI contrast, as well as a preparation method and application thereof. The contrast is obtained by chlorinating 4,4'-stilbenedimethy

Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides

Lee, Yong Ho,Morandi, Bill

, p. 1016 - 1022 (2018/09/06)

Current methods for functional group interconversion have, for the most part, relied on relatively strong driving forces which often require highly reactive reagents to generate irreversibly a desired product in high yield and selectivity. These approaches generally prevent the use of the same catalytic strategy to perform the reverse reaction. Here we describe a catalytic functional group metathesis approach to interconvert, under CO-free conditions, two synthetically important classes of electrophiles that are often employed in the preparation of pharmaceuticals and agrochemicals—aroyl chlorides (ArCOCl) and aryl iodides (ArI). Our reaction design relies on the implementation of a key reversible ligand C–P bond cleavage event, which enables a non-innocent, metathesis-active phosphine ligand to mediate a rapid aryl group transfer between the two different electrophiles. Beyond enabling a practical and safer approach to the interconversion of ArCOCl and ArI, this type of ligand non-innocence provides a blueprint for the development of a broad range of functional group metathesis reactions employing synthetically relevant aryl electrophiles.

Method of manufacturing imidoyl diazidosulfochloride compd. various compd. and manufacturing method of using the same

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Paragraph 0035, (2016/12/16)

PROBLEM TO BE SOLVED: To provide a new production method for synthesizing an imidoyl chloride compound dispensing with chlorination agents having poor handleability, to provide a method for producing various compounds in high yield and purity by using the imidoyl chloride compound, and to provide a method for isolating the imidoyl chloride compound in high efficiency and purity from a mixture of the imidoyl chloride compound and a phthalic anhydride compound.SOLUTION: The method for producing the imidoyl chloride compound comprises reaction of a specific amide compound with a specific phthaloyl chloride compound to produce a specific imidoyl chloride compound.

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