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34586-43-1

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34586-43-1 Usage

General Description

2-Ethylbenzenesulphonyl chloride is a chemical compound that is commonly used as an intermediate in the production of pharmaceuticals, dyes, and agrochemicals. It is a derivative of benzenesulphonyl chloride, with an ethyl group attached to the aromatic ring. 2-ETHYLBENZENESULPHONYL CHLORIDE is highly reactive and is often used as a reagent in organic synthesis to introduce the sulphonyl chloride functional group into various organic molecules. It is important to handle 2-ethylbenzenesulphonyl chloride with care, as it is corrosive and can cause severe irritation to the skin, eyes, and respiratory system if not properly handled. Additionally, it should be stored in a cool, dry place away from sources of ignition and incompatible materials.

Check Digit Verification of cas no

The CAS Registry Mumber 34586-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34586-43:
(7*3)+(6*4)+(5*5)+(4*8)+(3*6)+(2*4)+(1*3)=131
131 % 10 = 1
So 34586-43-1 is a valid CAS Registry Number.

34586-43-1SDS

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 2-Ethylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2-Ethylbenzenesulphonyl chloride

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:34586-43-1 SDS

34586-43-1Relevant articles and documents

Nitrene transfer catalyzed by a non-heme iron enzyme and enhanced by non-native small-molecule ligands

Goldberg, Nathaniel W.,Knight, Anders M.,Zhang, Ruijie K.,Arnold, Frances H.

supporting information, p. 19585 - 19588 (2019/12/24)

Transition-metal catalysis is a powerful tool for the construction of chemical bonds. Here we show that Pseudomonas savastanoi ethylene-forming enzyme, a non-heme iron enzyme, can catalyze olefin aziridination and nitrene C-H insertion, and that these activities can be improved by directed evolution. The non-heme iron center allows for facile modification of the primary coordination sphere by addition of metal-coordinating molecules, enabling control over enzyme activity and selectivity using small molecules.

Endothelin receptor antagonists

-

, (2008/06/13)

Novel compounds of the formula I STR1 in which R 1, R 2, R 3, --A B--C D--, Ar and X have the meaning indicated in claim 1, and their salts show endothelin receptor-antagonistic properties.

NATHAN-BAKER EFFECTS IN THE HETEROGENEOUS SULFONATION OF ALKYLBENZENES

Krylov, E. N.,Khokhlova, S. G.

, p. 341 - 343 (2007/10/02)

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