(3,5-Diphosphonophenyl)phosphonic acid

Base Information

Chemical Name:(3,5-Diphosphonophenyl)phosphonic acid
CAS No.:4672-29-1
Molecular Formula:C₆H₉O₉P₃
Molecular Weight:318.053
Hs Code.:
European Community (EC) Number:807-504-7
Nikkaji Number:J1.751.846A
Mol file:4672-29-1.mol

Synonyms:(3,5-diphosphonophenyl)phosphonic acid;4672-29-1;benzene-1,3,5-triyltris(phosphonic acid);SCHEMBL20379784;Benzene-1,3,5-trisphosphonic acid;YSZC888;1,3,5-benzenetriphosphonic acid;benzene-1,3,5-triphosphonic acid;MFCD22200395;(3,5-diphosphonophenyl)phosphonicacid;AKOS017345052;CS-0183001;F76987

Suppliers and Price of (3,5-Diphosphonophenyl)phosphonic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 9 raw suppliers

Chemical Property of (3,5-Diphosphonophenyl)phosphonic acid

Chemical Property:

XLogP3:-4
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:3
Exact Mass:317.94594285
Heavy Atom Count:18
Complexity:365

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C=C(C=C1P(=O)(O)O)P(=O)(O)O)P(=O)(O)O
General Description 1,3,5-Benzenetriphosphonic acid (BTPA), also referred to as benzene-1,3,5-triphosphonic acid (BTP or H₆bpt), is a phosphonate-based organic compound featuring three phosphonic acid groups symmetrically attached to a benzene ring. It serves as a versatile ligand in coordination chemistry and materials science, enabling the synthesis of metal-organic frameworks (MOFs) and hybrid materials with applications in optoelectronics and adsorption. For instance, it reacts with titanium(IV) isopropoxide to form thermally stable mesoporous titanium phosphonate nanomaterials (e.g., HTiP-7) with high surface area and photocurrent generation capabilities. Additionally, it forms layered copper phosphonates when combined with copper oxide and N-donor ligands, as well as hydrogen-bonded networks with organic bases like 4-(dimethylamino)pyridine, yielding 2D or 3D supramolecular architectures. These properties highlight its utility in designing functional crystalline materials.

Technology Process of (3,5-Diphosphonophenyl)phosphonic acid

There total 5 articles about (3,5-Diphosphonophenyl)phosphonic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.4%

: 449764-33-4
hexamethyl (benzene-1,3,5-triyl)tris[phosphonate]

: 4672-29-1
(benzene-1,3,5-triyl)tris[phosphonic acid]

Guidance literature:: With hydrogenchloride; In water; for 10h; Heating;
DOI:10.1002/1522-2675(200204)85:4<1140::AID-HLCA1140>3.0.CO;2-X

Reference yield: 92.0%

: 99624-20-1
hexaethyl benzene-1,3,5-tris(phosphonate)

: 4672-29-1
(benzene-1,3,5-triyl)tris[phosphonic acid]

Guidance literature:: With hydrogenchloride; water; for 12h;
DOI:10.1039/c3dt32744b

Reference yield: 92.0%

: 626-39-1
1,3,5-trisbromobenzene

: 4672-29-1
(benzene-1,3,5-triyl)tris[phosphonic acid]

Guidance literature:: 1,3,5-trisbromobenzene; With nickel dibromide; at 70 - 180 ℃; Inert atmosphere;

With triethyl phosphite; for 3h; Inert atmosphere;
DOI:10.1039/c3ta12476b