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"Benzenesulfonamide, 4-[[(4-hydroxy-3-methoxyphenyl)methylene]amino]-" is a complex organic compound with the chemical formula C14H14N2O4S. It is a derivative of benzenesulfonamide, featuring a 4-hydroxy-3-methoxyphenyl group connected to the benzene ring through an imine linkage. benzenesulfonamide, 4-[[(4-hydroxy-3-methoxyphenyl)methylene]amino]- is known for its potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of various drugs. Its structure provides a foundation for further chemical modifications, which can lead to the development of new therapeutic agents. The compound's specific properties and reactivity make it a valuable component in the field of medicinal chemistry, where it can be used to create compounds with specific biological activities.

2066-92-4

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2066-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2066-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2066-92:
(6*2)+(5*0)+(4*6)+(3*6)+(2*9)+(1*2)=74
74 % 10 = 4
So 2066-92-4 is a valid CAS Registry Number.

2066-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N4-(3-methoxy-4-hydroxybenzylidene) sulfanilamide

1.2 Other means of identification

Product number -
Other names N-Vanillyliden-sulfanilsaeure-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:2066-92-4 SDS

2066-92-4Downstream Products

2066-92-4Relevant academic research and scientific papers

Sulfanilamide benzaldehyde derivative preparation method

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Paragraph 0037; 0038, (2017/05/10)

The invention relates to an antigen material preparation method, and concretely relates to a sulfanilamide benzaldehyde derivative preparation method. The method comprises the following steps: taking sulfanilamide, and dissolving sulfanilamide in a solven

Carbonic anhydrase inhibitors. Part 35. Synthesis of Schiff bases derived from sulfanilamide and aromatic aldehydes: The first inhibitors with equally high affinity towards cytosolic and membrane-bound isozymes

Supuran,Nicolae,Popescu

, p. 431 - 438 (2007/10/03)

A series of Schiff bases was prepared by reaction of sulfanilamide with substituted benzene- and heterocyclic aldehydes. The compounds were characterized by standard procedures, and were assayed as inhibitors of the zinc enzyme carbonic anhydrase (CA). Th

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