Welcome to LookChem.com Sign In|Join Free

CAS

  • or

72305-02-3

Post Buying Request

72305-02-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

72305-02-3 Usage

Description

[(propan-2-yloxy)carbonyl]phosphonic acid, also known as isobutylidenebisphosphonic acid, is a chemical compound with the molecular formula C5H11O6P. It is a phosphonic acid derivative that possesses the ability to form stable complexes with metal ions, making it a versatile compound with various applications in industrial and therapeutic fields.

Uses

Used in Water Treatment Processes:
[(propan-2-yloxy)carbonyl]phosphonic acid is used as a chelating agent for the purpose of sequestering metal ions in water treatment processes. Its ability to form stable complexes with metal ions helps in preventing scale formation, corrosion, and fouling in water systems.
Used in Cleaning Products:
In the cleaning industry, [(propan-2-yloxy)carbonyl]phosphonic acid is used as a sequestering agent to enhance the effectiveness of cleaning products. Its chelating properties allow it to bind with metal ions, preventing them from interfering with the cleaning process and improving the overall performance of the product.
Used in Corrosion Inhibition:
[(propan-2-yloxy)carbonyl]phosphonic acid is used as a corrosion inhibitor in various industrial applications. Its ability to form stable complexes with metal ions helps in reducing the rate of corrosion, thereby protecting equipment and infrastructure from damage.
Used in Pharmaceutical Applications:
[(propan-2-yloxy)carbonyl]phosphonic acid has been studied for its potential therapeutic applications, particularly in the treatment of bone-related diseases such as osteoporosis and Paget's disease. Its ability to inhibit bone resorption makes it a promising candidate for the development of new drugs to combat these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 72305-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,0 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72305-02:
(7*7)+(6*2)+(5*3)+(4*0)+(3*5)+(2*0)+(1*2)=93
93 % 10 = 3
So 72305-02-3 is a valid CAS Registry Number.

72305-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yloxycarbonylphosphonic acid

1.2 Other means of identification

Product number -
Other names Disodium i-propoxycarbonylphosphonate

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:72305-02-3 SDS

72305-02-3Downstream Products

72305-02-3Relevant articles and documents

Synthesis of esters of phosphonoformic acid and their antiherpes activity

Noren,Helgstrand,Johansson,Misiorny,Stening

, p. 264 - 270 (2007/10/02)

Aliphatic and aromatic mono-, di-, and triesters of phosphonoformic (foscarnet) were synthesized. The triesters were prepared by the Michaelis-Arbuzov reaction and were hydrolyzed to di- and monoesters. The compounds were tested for antiviral activity on isolated herpes simplex virus type 1 (HSV-1) DNA polymerase, in a HSV-1 plaque reduction assay, and on a cutaneous HSV-1 infection in guinea pigs. None of the esters inhibited the activity of isolated HSV-1 polymerases. Monoesters with a free carboxylic group and diesters with an aromatic carboxylic ester function were active against the cutaneous herpesa infection. Mono- and diesters with an aromatic phosphonic ester group also showed activity in the plaque-reduction assay. However, mono- and diesters with aliphatic carboxylic ester groups were inactive in all test systems. The results show that all three acidic groups of phosphonoformic acid must be free in order to get antiviral activity at the enzyme level. However, certain esters of this acid may be biotransformed to the acid itself to give antiherpes activity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 72305-02-3