142434-81-9 Usage
Description
4-Phosphonomethyl-L-Phenylalanine is a synthetic chemical compound that is primarily used in scientific research, particularly in the field of biochemistry. It is structurally similar to phenylalanine, an essential amino acid that forms proteins in the human body. 4-Phosphonomethyl-L-Phenylalanine exists as a white or off-white powder with the chemical formula C10H13NO5P and may also be utilized as a phosphonate, a class of chemicals often used in the formulation of flame retardants, corrosion inhibitors, and water softening products. However, its use is mainly restricted to laboratory research and it is not typically found in consumer products.
Uses
Used in Scientific Research:
4-Phosphonomethyl-L-Phenylalanine is used as a research compound for its structural similarity to phenylalanine, which aids in the study of protein formation and related biochemical processes.
Used in Biochemistry:
4-Phosphonomethyl-L-Phenylalanine is used as a biochemical tool to investigate the role of phenylalanine in protein synthesis and its potential applications in understanding various biological mechanisms.
Used in Flame Retardant Formulation:
Although its use is mainly restricted to laboratory research, 4-Phosphonomethyl-L-Phenylalanine is used as a phosphonate in the development of flame retardants, contributing to the creation of safer materials that resist ignition and slow the spread of fire.
Used in Corrosion Inhibition:
4-Phosphonomethyl-L-Phenylalanine is used as a phosphonate in the formulation of corrosion inhibitors, helping to protect materials from the damaging effects of corrosion and extending their lifespan.
Used in Water Softening Products:
As a phosphonate, 4-Phosphonomethyl-L-Phenylalanine is used in the development of water softening products, which are designed to reduce the hardness of water and prevent the buildup of mineral deposits in plumbing systems and appliances.
Check Digit Verification of cas no
The CAS Registry Mumber 142434-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,3 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142434-81:
(8*1)+(7*4)+(6*2)+(5*4)+(4*3)+(3*4)+(2*8)+(1*1)=109
109 % 10 = 9
So 142434-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14NO5P/c11-9(10(12)13)5-7-1-3-8(4-2-7)6-17(14,15)16/h1-4,9H,5-6,11H2,(H,12,13)(H2,14,15,16)
142434-81-9Relevant articles and documents
Composition, synthesis and therapeutic applications of polyamines
-
, (2008/06/13)
This invention relates to a process of synthesis and composition of open chain (ring), closed ring, linear branched and or substituted polyamines, polyamine derived tyrosine phosphatase inhibitors and PPAR partial agonists/partial antagonists via a series of substitution reactions and optimizing the bioavailability and biological activities of the compounds. Polyamines prevent the toxicty of neutoxins and diabetogenic toxins including paraquat, methyphenyl pyridine radical, rotenone, diazoxide, streptozotocin and alloxan. These polyamines can be to treat neurological, cardiovascular, endocrine acquired and inherited mitochondrial DNA damage diseases and other disorders in mammalian subjects, and more specifically to the therapy of Parkinson's disease, Alzheimer's disease, Lou Gehrig's disease, Binswanger's disease, Olivopontine Cerebellar Degeneration, Lewy Body disease, Diabetes, Stroke, Atherosclerosis, Myocardial Ischemia, Cardiomyopathy, Nephropathy, Ischemia, Glaucoma, Presbycussis, Cancer, Osteoporosis, Rheumatoid Arthritis, Inflammatory Bowel Disease, Multiple Sclerosis and as Antidotes to Toxin Exposure.
Enantioselective synthesis of N-Fmoc protected di-tert-butyl 4-phosphonomethyl-L-phenylalanine: A hydrolytically stable analogue of O-phosphotyrosine
Liu,Roques,Garbay-Jaureguiberry
, p. 647 - 650 (2007/10/02)
Fmoc-L-Pmp(tBu)2-OH was prepared with high enantiomeric purity by an asymmetric synthetic pathway, using a camphor sultam as chiral auxiliary.
