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p-Chlor-benzoylaminoxy-essigsaeure, also known as 4-chlorobenzoyl-N-hydroxyl-acetic acid, is a chemical compound with the molecular formula C8H6ClNO4. It is a derivative of benzoic acid, featuring a chloro substituent at the para position, an amide group, and a hydroxyl group. p-Chlor-benzoylaminoxy-essigsaeure is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and pesticides. Its chemical structure allows for the formation of various esters and amides, which can be further modified to create active ingredients with specific properties. Due to its reactivity and potential applications, p-Chlor-benzoylaminoxy-essigsaeure is an important compound in the field of organic chemistry and chemical engineering.

5251-91-2

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5251-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5251-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5251-91:
(6*5)+(5*2)+(4*5)+(3*1)+(2*9)+(1*1)=82
82 % 10 = 2
So 5251-91-2 is a valid CAS Registry Number.

5251-91-2Relevant academic research and scientific papers

Design, synthesis and prostate cancer cell-based studies of analogs of the Rho/MKL1 transcriptional pathway inhibitor, CCG-1423

Evelyn, Chris R.,Bell, Jessica L.,Ryu, Jenny G.,Wade, Susan M.,Kocab, Andrew,Harzdorf, Nicole L.,Hollis Showalter,Neubig, Richard R.,Larsen, Scott D.

scheme or table, p. 665 - 672 (2010/06/21)

We recently identified bis(amide) CCG-1423 (1) as a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis. An initial structure-activity relationship study focusing on bioisosteric replacement of the amides and conformational restriction identified two compounds, 4g and 8, with improved selectivity for inhibition of RhoA/C-mediated gene transcription and attenuated cytotoxicity relative to 1. Both compounds were also capable of inhibiting cell invasion with equal efficacy to 1 but with less attendant cytotoxicity.

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