6056-52-6 Usage
Description
[(isopropylimino)dimethylene]bisphosphonic acid is a versatile chemical compound belonging to the bisphosphonate class, characterized by its two phosphonic acid groups and an iminomethylene group. It is recognized for its chelating properties, ability to bind metal ions, and regulate their activity in biological systems, making it a valuable asset in various applications.
Uses
Used in Pharmaceutical Industry:
[(isopropylimino)dimethylene]bisphosphonic acid is used as a therapeutic agent for treating conditions such as osteoporosis and other bone diseases. Its application is based on its effectiveness in inhibiting bone resorption and promoting bone health.
Used in Industrial Processes:
In the industrial sector, [(isopropylimino)dimethylene]bisphosphonic acid is used as a corrosion inhibitor. Its ability to bind metal ions helps protect materials from corrosion, extending their lifespan and improving efficiency.
Used in Water Treatment:
[(isopropylimino)dimethylene]bisphosphonic acid is also utilized in water treatment processes to prevent the formation of scale deposits. By chelating metal ions, it helps maintain the quality of water and prevents potential damage to water systems and appliances.
Used in Cancer Therapy:
[(isopropylimino)dimethylene]bisphosphonic acid has potential applications in cancer therapy due to its ability to inhibit bone resorption and tumor growth. Its chelating properties and regulation of metal ion activity contribute to its potential as a therapeutic agent in oncology.
Check Digit Verification of cas no
The CAS Registry Mumber 6056-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6056-52:
(6*6)+(5*0)+(4*5)+(3*6)+(2*5)+(1*2)=86
86 % 10 = 6
So 6056-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H28BrNO5/c1-5-33-21-12-8-18(9-13-21)26(17-6-10-20(30-2)11-7-17)28-25(29)15-19-14-23(31-3)24(32-4)16-22(19)27/h6-14,16,26H,5,15H2,1-4H3,(H,28,29)
6056-52-6Relevant articles and documents
Novel layered lead(II) aminodiphosphonates with carboxylate-sulfonate and 1,3,5-benzenetricarboxylate ligands as pendant groups or intercalated species
Ying, Shao-Ming,Mao, Jiang-Gao
, p. 1270 - 1276 (2007/10/03)
The hydrothermal reaction of lead(II) carbonate with 3-sulfobenzoic acid, 3-HO3S-C6H4-CO2H, and isopropylimino-bis(methylenephosphonic acid), (CH3) 2CHN(CH2PO3H2)2 (H 4L1), gave a new layered lead(II) carboxylate-phosphonate, Pb7(S-O3S-C6H4-CO 2)(L1)3(H2O)2· 2H2O (1), whereas the hydrothermal reaction of lead(II) carbonate with 1, 3,5-benzenetricarboxylic acid (H3BTC) and N-cyclohexyUmino-bis(methylenephosphonic acid), C6H 11N(CH2PO3H2)2 (H 4L2), afforded a layered complex, Pb3(HL 2)(H2L2)(H2BTC)-(H 2O)·H3BTC·H2O (2). The structure of complex 1 contains 〈010〈 lead(II) carboxylate-phosphonate hybrid layers, with the sulfonate group of the carboxylate-sulfonate ligand as the pendant group. In complex 2, the lead(II) ions are interconnected through bridging diphosphonate ligands, and results in the formation of a lead(II) diphosphonate slab, which are further interlinked via hydrogen bonds between non-coordinated phosphonate oxygen atoms to form a 〈001〈 layer. The doubly protonated H2BTC anion is bidentately chelated to a lead(II) ion through a carboxylate group, whereas the neutral H3BTC ligand is intercalated between two layers, forming hydrogen bonds with the non-coordinated carboxylate groups of the H2BTC anion. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
