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N-[(Ethylamino)carbonyl]-4-methylbenzenesulfonamide, also known as ethyl 4-methylbenzenesulfonamide, is a chemical compound with the molecular formula C10H14N2O3S. It is a white crystalline solid that is soluble in water and various organic solvents. N-[(Ethylamino)carbonyl]-4-methylbenzenesulfonamide is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its versatile reactivity and can be further functionalized to produce a range of derivatives with different properties and applications. The compound is also recognized for its potential role in chemical research, particularly in the development of new drug candidates and the exploration of novel chemical reactions.

1467-23-8

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1467-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1467-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1467-23:
(6*1)+(5*4)+(4*6)+(3*7)+(2*2)+(1*3)=78
78 % 10 = 8
So 1467-23-8 is a valid CAS Registry Number.

1467-23-8SDS

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 1-ethyl-3-(4-methylphenyl)sulfonylurea

1.2 Other means of identification

Product number -
Other names N-Ethyl-N'-toluene-p-sulfonylurea

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:1467-23-8 SDS

1467-23-8Downstream Products

1467-23-8Relevant academic research and scientific papers

A facile synthesis of sulfonylureas: Via water assisted preparation of carbamates

Tanwar, Dinesh Kumar,Ratan, Anjali,Gill, Manjinder Singh

, p. 4992 - 4999 (2017/07/11)

A novel and simple approach to the synthesis of sulfonylureas has been reported. It involved the reaction of various amines with diphenyl carbonate to yield the corresponding carbamates, which subsequently reacted with different sulphonamides to produce different sulfonylureas in excellent yields. The first reaction of diphenyl carbonate with amines was carried out in aqueous:organic (H2O:THF, 90:10) medium at room temperature to produce carbamates that paved a straightforward route to sulfonylureas after reaction with sulfonamides. The above process avoided traditional multistep protocols and the use of hazardous, irritant, toxic and moisture sensitive reagents such as phosgene, isocyanates and/or chloroformates.

An improved method for the synthesis of sulfonylureas

Cervello,Sastre

, p. 221 - 222 (2007/10/02)

Treatment of isocyanates with sulfonamides in dimethylformamide in the presence of copper(I) chloride affords sulfonylureas in high yields under mild conditions.

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