14596-56-6 Usage
Uses
Used in Chemical Synthesis:
(2-(Dimethylamino)ethyl)phosphonic acid is used as a synthetic building block for the development of various organic compounds and pharmaceuticals. Its unique structure allows for versatile chemical reactions and the formation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-(dimethylamino)ethyl)phosphonic acid is used as an intermediate in the synthesis of drugs with potential therapeutic applications. Its ability to form stable complexes with biological targets makes it a valuable component in the development of new medications.
Used in Material Science:
(2-(Dimethylamino)ethyl)phosphonic acid can be utilized in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties. Its incorporation into these materials can enhance their performance characteristics, such as durability, stability, and reactivity.
Used in Environmental Applications:
(2-(Dimethylamino)ethyl)phosphonic acid may also find use in environmental applications, such as water treatment and soil remediation. Its ability to form complexes with metal ions can help in the removal of contaminants and the improvement of environmental conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 14596-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,9 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14596-56:
(7*1)+(6*4)+(5*5)+(4*9)+(3*6)+(2*5)+(1*6)=126
126 % 10 = 6
So 14596-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H12NO3P/c1-5(2)3-4-9(6,7)8/h3-4H2,1-2H3,(H2,6,7,8)
14596-56-6Relevant academic research and scientific papers
A new simple route to N-substituted 2-aminoethylphosphonic acids
Fu, Xiangkai,Gong, Chengbin,Ma, Xuebing,Wen, Shuying
, p. 2659 - 2664 (2007/10/03)
2-Aminoethylphosphonic acid (AEPA) and its N-substituted compounds were prepared by one step reaction using 2-chloroethylphosphonic acid with ammonia and amines (H2NMe, HNMeMe, HNEtEt, H2NPr-n, H2NCH2ph,H2NCH2CH2NH2 and H2N(C=NH)NH2 in a dilute alkaline solution below 20 °C with simple work- up and easy purification. The reaction was accelerated by catalytic amount of potassium iodide. The yield for the reaction products were 35.6 to 48.6% for the KI absence and 78.2 to 88.0% for the KI presence.
AMINATION REDUCTRICE D'ALDEHYDES PHOSPHONIQUES. Un Reexamen
Collignon, N.,Fabre, G.,Varlet, J. M.,Savignac, Ph.
, p. 81 - 86 (2007/10/02)
The reactivity of diethyl-2-oxo ethyl- and 3-oxo propylphosphonates with ammonia, methyl and dimethylamine at pH 7 in the presence of sodium cyanohydridoborate via reductive amination of the carbonyl group has been reexamined.Reactions of diethyl-2-oxoethyl- and 3-oxopropylphosphonates with ammonia give imino-bis-(alkylphosphonates); methyl and dimethylamine give monocondensation products thus permitting the synthesis of N-substituted aminoalkylphosphonates.
