109638-78-0 Usage
Description
(R)-1-Aminoheptylphosphonic acid, also known as (R)-AHPC, is a versatile organophosphorus compound that belongs to the class of phosphonate compounds. It features a phosphonic acid group and an amino group, which contribute to its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Uses
Used in Chelating Applications:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a chelating agent for its ability to form stable complexes with metal ions. This property makes it useful in various industrial processes, such as water treatment and the removal of metal contaminants.
Used in Pharmaceutical Synthesis:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential applications in treating a range of medical conditions.
Used in Agrochemical Synthesis:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a building block in the creation of novel agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can lead to improved efficacy and reduced environmental impact.
Used in Corrosion Inhibition:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a corrosion inhibitor for its ability to protect metal surfaces from degradation. This application is particularly relevant in the oil and gas industry, where corrosion-resistant materials are crucial for maintaining the integrity of pipelines and storage tanks.
Used in Neurological Disorder Treatment:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a potential treatment for certain neurological disorders due to its interactions with specific receptors and enzymes in the nervous system. Further research is needed to fully understand its therapeutic potential and optimize its use in this context.
Used in Research and Development:
(R)-1-AMINOHEXYLPHOSPHONIC ACID is used as a versatile compound in research and development settings, where its unique properties can be harnessed to explore new chemical reactions, materials, and applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 109638-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,6,3 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109638-78:
(8*1)+(7*0)+(6*9)+(5*6)+(4*3)+(3*8)+(2*7)+(1*8)=150
150 % 10 = 0
So 109638-78-0 is a valid CAS Registry Number.
109638-78-0Relevant articles and documents
ORGANOPHOSPHORUS COMPOUNDS AS POTENTIAL FUNGICIDES. PART II. AMINOALKANE-, GUANIDINOALKANE-, AND THIOUREIDOALKANE-PHOSPHONIC ACIDS: PREPARATION, SPECTROSCOPY, AND FUNGICIDAL ACTIVITY
Cameron, David G.,Hudson, Harry R.,Pianka, Max
, p. 21 - 38 (2007/10/02)
A range of α-amino-, ω-amino-, α-guanidino-, and ω-guanidinoalkanephosphonic acids has been prepared for the purpose of studying their spectroscopic features and fungicidal activity.In addition, α-thioureido-octanephosphonic acid and thioureylene-1,1-bis(1-octanephosphonic acid) were isolated during the preparation of α-guanidino-octanephosphonic acid. 31P, 1H, and 13C nmr spectral data which were obtained for solutions of the amino- and guanidino-compounds in D2O or D2O/D2SO4, and for the thioureido compounds in DMSO-d6, are discussed together with previouslyreported data for the aminophosphonic types.FAB mass spectrometry generally gives strong pseudomolecular ions + for the zwitterionic amino- and guanidino-compounds with relatively simple fragmentations.Fungicidal activity of the α-aminophosphonic acids was found to be greater than for the ω-amino compounds, with maximum activity at a chain length of three carbon atoms when used as a seed dressing for the control of Drechslera spp.Moderately good activity was shown by the thioureido compounds against a number of fungal organisms in vitro but the guanidino-compounds exhibited low activity.Key words: Organophosphorus; fungicides; aminophosphonic acids; guanidinophosphonic acids; NMR spectroscopy; FAB mass spectroscopy.
Synthesis of O,O-Dialkyl 1-Aminoalkanephosphonates
Kudzin, Z.H.,Kotynski, A.
, p. 1028 - 1032 (2007/10/02)
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