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The chemical "4-({[(1E,4E)-4-([4-(diethylamino)phenyl]{4-[ethyl(4-sulfonatobenzyl)amino]phenyl}methylidene)cyclohexa-2,5-dien-1-ylidene](ethyl)ammonio}methyl)benzenesulfonate" is a complex organic compound with a molecular formula of C38H44N4O6S2. It is characterized by a benzene ring with a sulfonate group attached, and a long, conjugated side chain that includes a cyclohexadienyl moiety, multiple nitrogen atoms in various amine and amide configurations, and a diethylamino group. 4-({[(1E,4E)-4-([4-(diethylamino)phenyl]{4-[ethyl(4-sulfonatobenzyl)amino]phenyl}methylidene)cyclohexa-2,5-dien-1-ylidene](ethyl)ammonio}methyl)benzenesulfonate is notable for its intricate structure, which features a combination of aromatic, aliphatic, and heterocyclic components, as well as charged groups that could influence its reactivity and solubility properties. The specific arrangement of these functional groups suggests potential applications in areas such as pharmaceuticals, dyes, or materials science, where complex molecular structures are often associated with specific functionalities.

5573-22-8

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5573-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5573-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5573-22:
(6*5)+(5*5)+(4*7)+(3*3)+(2*2)+(1*2)=98
98 % 10 = 8
So 5573-22-8 is a valid CAS Registry Number.

5573-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-[[4-(diethylamino)phenyl]-[4-[ethyl-[(4-sulfonatophenyl)methyl]azaniumylidene]cyclohexa-2,5-dien-1-ylidene]methyl]-N-ethylanilino]methyl]benzenesulfonate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5573-22-8 SDS

5573-22-8Upstream product

5573-22-8Downstream Products

5573-22-8Relevant academic research and scientific papers

Synthesis and biological activities of substituted glycyrrhetic acids

Baran,Langford,Liang,Pitzele

, p. 184 - 191 (2007/10/15)

18β Glycyrrhetic acid (I) was converted in good yield to a 3 oxo 4,4 bis (nor 18β olean 4 ene) derivative in 25% overall yield. Derivatives of I substituted in the A, B, C, and E rings were also prepared. Several 11 deoxoglycyrrhetic acid derivatives exhibited desoxycortone antagonism. In particular, when administered subcutaneously, 3 oxo 18β olean 12 en 30 oic acid had about 75% the activity of spironolactone administered subcutaneously. Several compounds also exhibited weak antiviral and antiinflammatory properties.

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