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5251-93-4

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5251-93-4 Usage

Description

BENZADOX, also known as hippurate analog, is a pale yellow solid with unique chemical properties. It is recognized for its ability to inhibit peptidylglycine α-hydroxylating monooxygenase (PHM), making it a potential candidate for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
BENZADOX is used as an inhibitor for peptidylglycine α-hydroxylating monooxygenase (PHM) for its potential role in the development of new therapeutic strategies and treatments. Its ability to inhibit PHM can be beneficial in the research and development of drugs targeting specific enzyme-related conditions.
Used in Agricultural Industry:
BENZADOX is used as a pesticide for its ability to control and manage pests in the agricultural sector. Its effectiveness in inhibiting certain biological processes makes it a valuable tool in protecting crops and ensuring a healthy yield.
Used in Chemical Research:
BENZADOX, being a hippurate analog, is used as a research compound in the field of chemical research. Its unique properties and ability to inhibit PHM make it an interesting subject for further study and potential development of new chemical compounds and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5251-93-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 5251-93:
(6*5)+(5*2)+(4*5)+(3*1)+(2*9)+(1*3)=84
84 % 10 = 4
So 5251-93-4 is a valid CAS Registry Number.
InChI:InChI=1S/C9H9NO4/c11-8(12)6-14-10-9(13)7-4-2-1-3-5-7/h1-5H,6H2,(H,10,13)(H,11,12)

5251-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzadox

1.2 Other means of identification

Product number -
Other names 2-[(benzoylamino)oxy]acetic acid

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:5251-93-4 SDS

5251-93-4Relevant articles and documents

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.

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

-

, (2008/06/13)

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.

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