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"N~2~-[(4-methylphenyl)sulfonyl]-N-phenylglutamine" is a complex organic compound with the molecular formula C18H20N2O4S. It features a glutamine backbone, which is an amino acid, with a phenyl group attached to the nitrogen atom at the second position (N2). Additionally, a 4-methylphenylsulfonyl group is connected to the same nitrogen, introducing a sulfonyl functional group and a methyl-substituted phenyl ring. N~2~-[(4-methylphenyl)sulfonyl]-N-phenylglutamine is known for its potential applications in pharmaceuticals, particularly as a building block in the synthesis of certain drugs. Its structure provides a balance of hydrophilic and hydrophobic characteristics, which can be crucial for its interaction with biological targets. The sulfonyl group may contribute to the compound's reactivity or stability in chemical transformations, while the phenyl groups can influence its lipophilicity and potential for binding to protein targets.

7460-91-5

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7460-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7460-91-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7460-91:
(6*7)+(5*4)+(4*6)+(3*0)+(2*9)+(1*1)=105
105 % 10 = 5
So 7460-91-5 is a valid CAS Registry Number.

7460-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-anilino-2-[(4-methylphenyl)sulfonylamino]-5-oxopentanoic acid

1.2 Other means of identification

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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

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More Details:7460-91-5 SDS

7460-91-5Relevant academic research and scientific papers

Synthesis and Antineoplastic Activity of 5-N-Alkyl-2-p-substituted-benzenesulphonyl-L-glutamines

De, A. U.,Pandey, Jiten,Majumdar, Anjali

, p. 481 - 483 (2007/10/02)

5-N-Alkyl-2-p-substituted-benzenesulphonyl-l-glutamines (III) have been synthesised and their antineoplastic potency evaluated in Ehrlich ascites carcinoma (EAC) in Swiss albino mice.A few of the compounds show appreciable activity.An interesting phenomenon of C-N bond cleavage has been observed when 2-p-toluenesulphonyl-L-glutamine (III; X = CH3, R = H) is treated with PPA.

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