17261-34-6

Usage

Uses

Used in Chemical Synthesis:
IMINO-BIS(METHYLPHOSPHONIC ACID) is used as a complex-forming reagent for [alkylphosphonic groups] to facilitate the preparation of new synthons. This is important for designing polyfunctional chelating agents with various coordination centers, which can be utilized in a range of chemical applications and industries.
Used in Research and Development:
In the field of research and development, IMINO-BIS(METHYLPHOSPHONIC ACID) serves as a valuable compound for creating novel chelating agents. These agents can be applied in various areas, such as catalysis, environmental remediation, and pharmaceutical development, due to their ability to form stable complexes with metal ions.
Used in Pharmaceutical Industry:
IMINO-BIS(METHYLPHOSPHONIC ACID) is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique properties allow for the development of new drugs with potential applications in treating various diseases and medical conditions.
Used in Environmental Applications:
The complex-forming ability of IMINO-BIS(METHYLPHOSPHONIC ACID) makes it a candidate for use in environmental applications, such as the removal of heavy metals from contaminated water or soil. By chelating with metal ions, it can help to reduce the toxicity and mobility of these pollutants, aiding in their removal and cleanup efforts.

InChI:InChI=1/C2H9NO6P2/c4-10(5,6)1-3-2-11(7,8)9/h3H,1-2H2,(H2,4,5,6)(H2,7,8,9)

Upstream product

• 2439-99-8 <<(carboxymethyl)imino>dimethylene>bisphosphonic acid 
• 50-00-0 formaldehyd 
• 120060-75-5 N-(triphenylmethyl)methanimine 
• 108-24-7 acetic anhydride 
• 142-73-4 iminodiacetic acid 
• 100-97-0 hexamethylenetetramine 
• 6419-19-8 nitrilo-tris(methylenephosphonic acid) 
• 69028-54-2 tetraethyl [iminodi(methylene)]bis(phosphonate) 

Downstream Products

• 5995-25-5 N-methyliminobis(methylphosphonic acid) 
• 2439-99-8 <<(carboxymethyl)imino>dimethylene>bisphosphonic acid 
• 54622-43-4 2-hydroxypropylene-1,3-diamino-N,N,N',N'-tetramethylenephosphonic acid 
• 5995-42-6 <(2-hydroxyethyl)imino>dimethylene diphosphonic acid 

Relevant academic research and scientific papers

METHOD FOR THE SYNTHESIS OF ALPHA-AMINOALKYLENEPHOSPHONIC ACID

The present invention is related to a new method for the synthesis of alpha-aminoalkylenephosphonic acid or its phosphonate esters comprising the steps of forming a reaction mixture by mixing a P-O-P anhydride moiety comprising compound, having one P-atom at the oxidation state (+111) and the other P-atom at the oxidation state (+111) or (+V), an aminoalkanecarboxylic acid and an acid catalyst, wherein said reaction mixture comprises an equivalent ratio of alpha-aminoalkylene carboxylic acid to P-O-P anhydride moieties of at least 0.2, and recovering the resulting alpha-aminoalkylene phosphonic acid compound or an ester thereof from the reaction mixture.

Tritylamine (triphenylmethylamine) in organic synthesis; III. The synthesis of 1-aminoalkylphosphonic acids in the reaction of N-(triphenylmethyl) alkanimines with phosphorus trichloride in acetic acid or with phosphonic (phosphorous) acid in acetic anhydride

The reaction of phosphorus trichloride in acetic acid or phosphonic (phosphorous) acid in acetic anhydride, with N-(triphenylmethyl)alkanimines gives 1-acetylaminoalkylphosphonic acids 1a-j, which after hydrolysis give 1-aminoalkylphosphonic acids 2a-j in good yields. ARKAT USA, Inc.

Hydrothermal synthesis and crystal structure of two Co phosphonates containing trifunctional phosphonate anions: Co3(O 3PCH2NH2CH2PO3) 2 and Co3(O3PCH2

Two cobalt phosphonates containing trifunctional phosphonate anions have been synthesised and their structures solved by single crystal diffraction. Co3(O3PCH2NH2CH2PO 3)2 (3) wa