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Glycine, N-phenyl-N-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59724-82-2

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59724-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59724-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59724-82:
(7*5)+(6*9)+(5*7)+(4*2)+(3*4)+(2*8)+(1*2)=162
162 % 10 = 2
So 59724-82-2 is a valid CAS Registry Number.

59724-82-2Downstream Products

59724-82-2Relevant academic research and scientific papers

Ramoplanin derivatives possessing antibacterial activity

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Page/Page column 39; 53, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

N- and 2-Substituted N-(Phenylsulfonyl)glycines as Inhibitors of Rat Lens Aldose Reductase

DeRuiter, Jack,Borne, Ronald F.,Mayfield, Charles A.

, p. 145 - 151 (2007/10/02)

A variety of N-(phenylsulfonyl)-N-phenylglycines 5, N-(phenylsulfonyl)-2-phenylglycines 6, and N-(phenylsulfonyl)anthranilic acids 7 were prepared as analogues of the N-(phenylsulfonyl)glycine 1 aldose reductase inhibitors.In the rat lens assay, several derivatives of 5 display greater inhibitory activity than the corresponding glycines 1, suggesting that N-phenyl substitution enhances affinity for aldose reductase.Enzyme kinetic evaluations of the 4-benzoylamino analogues of 5 and 1 demonstrate that these compounds produce inhibition by the same mechanism.However, the significant differences in relative inhibitory potencies between compounds of series 5 and 1 may indicate that these compounds do not interact with the inhibitor binding site in precisely the same manner.Evaluation of the individual enantiomers of series 6 reveals that the S isomers are substantially more active than the corresponding R isomers.Also, with the exception of the naphthalene analogue 6n, the S stereoisomers of this series display greater inhibitory potencies than the glycines 1.The anthranilates 7 generally are less active than the glycines 1, demonstrating that direct incorporation of an aromatic ring in the glycine side chain may result in a decrease in affinity for aldose reductase.

Method for controlling the growth of plants

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, (2008/06/13)

A method for controlling the growth of plants, characterized by applying a plant growth regulator containing as active ingredient a benzenesulfonamide derivative represented by the general formula, STR1 wherein X is a halogen atom, an alkyl group having 1

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