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Benzenesulfonamide, 2,5-dichloro-N,N-dimethyl-, also known as 2,5-Dichloro-N,N-dimethylbenzenesulfonamide, is a chemical compound with the molecular formula C8H9Cl2NO2S. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 260.13 g/mol. Benzenesulfonamide, 2,5-dichloro-N,N-dimethyl- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. It is characterized by its two chlorine atoms at the 2nd and 5th positions on the benzene ring, as well as two methyl groups attached to the nitrogen atom in the sulfonamide group. Due to its reactivity and potential applications, it is essential to handle Benzenesulfonamide, 2,5-dichloro-N,N-dimethyl- with care, following proper safety protocols and guidelines.

88522-19-4

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88522-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88522-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88522-19:
(7*8)+(6*8)+(5*5)+(4*2)+(3*2)+(2*1)+(1*9)=154
154 % 10 = 4
So 88522-19-4 is a valid CAS Registry Number.

88522-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dichloro-N,N-dimethylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-2.5-dichlor-benzolsulfonsaeure-amid

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:88522-19-4 SDS

88522-19-4Downstream Products

88522-19-4Relevant academic research and scientific papers

An approach to C-N activation: Coupling of arenesulfonyl hydrazides and arenesulfonyl chlorides with: Tert -amines via a metal-, oxidant- and halogen-free anodic oxidation

Sheykhan,Khani,Abbasnia,Shaabanzadeh,Joafshan

, p. 5940 - 5948 (2017/12/26)

tert-Amines were harnessed to afford arenesulfonyl hydrazides and arenesulfonyl chlorides via a metal-, oxidant- and halogen-free electrochemical oxidative coupling in an undivided cell at RT. This environmentally benign approach afforded a wide spectrum of sulfonamides in satisfactory yields using cheap and renewable Pencil Graphite Electrodes (PGEs).

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