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4-CARBOXYPHENYLPHOSPHONIC ACID, also known as 4-Phosphonobenzoic Acid, is an organic compound with the molecular formula C7H7O4P. It is characterized by its phosphonic acid functional group, which gives it unique chemical properties and reactivity. 4-CARBOXYPHENYLPHOSPHONIC ACID has been found to possess various biological activities, making it a versatile molecule with potential applications in different fields.

618-21-3

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618-21-3 Usage

Uses

Used in Pharmaceutical Industry:
4-CARBOXYPHENYLPHOSPHONIC ACID is used as an antifibrinolytic agent for its ability to inhibit the breakdown of fibrin, a key component in blood clotting. This property makes it useful in the treatment of conditions where excessive bleeding is a concern, such as during surgery or in cases of trauma.
Additionally, 4-CARBOXYPHENYLPHOSPHONIC ACID is used as an antibacterial agent due to its ability to inhibit bacterial growth. This application can be particularly useful in the development of new antibiotics to combat drug-resistant bacterial strains.

Check Digit Verification of cas no

The CAS Registry Mumber 618-21-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 618-21:
(5*6)+(4*1)+(3*8)+(2*2)+(1*1)=63
63 % 10 = 3
So 618-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7O5P/c8-7(9)5-1-3-6(4-2-5)13(10,11)12/h1-4H,(H,8,9)(H2,10,11,12)

618-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phosphonobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-phosphono

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:618-21-3 SDS

618-21-3Relevant academic research and scientific papers

A novel approach to phosphonic acids from hypophosphorous acid

Bravo-Altamirano, Karla,Montchamp, Jean-Luc

, p. 5755 - 5759 (2008/02/09)

A novel access to phosphonic acids via Pd-catalyzed tandem carbon-phosphorus bond formation-oxidation processes was developed. The procedures involve atom-economical and environmentally friendly functionalization reactions of hypophosphorous acid (H3PO2) and H-phosphinic acids [RP(O)(OH)(H)].

Palladium-catalyzed arylation of diethyl phosphonate in aqueous-organic media

Beletskaya,Kabachnik,Solntseva

, p. 71 - 73 (2007/10/03)

Diethyl arylphosphonates were synthesized by reactions of diethyl phosphonate with aryl iodides or bromides containing electron-donor or electron-acceptor substituents in the aromatic ring in aqueous acetonitrile or neat water in the presence of palladium

Arylphosphonic acids. I. Substituent effects on their first and second dissociations

Nagarajan, K.,Shelly, Kevin P.,Perkins, R. R.,Stewart, Ross

, p. 1729 - 1733 (2007/10/02)

Thermodynamic pK1 and pK2 values of 36 arylphosphonic acids have been determined.The pK values of the meta and para compounds are correlated well by the ?n parameter, suggesting that there is little conjugation between the

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