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Phosphonic acid, [(3-fluorophenyl)methyl]-, also known as a phosphonic acid derivative, is a chemical compound characterized by the molecular formula C7H8FOP. It features a fluorophenylmethyl group attached to the phosphorus atom, which endows it with unique structural and reactivity properties. These attributes make it a versatile intermediate in organic synthesis and a valuable building block in the production of pharmaceuticals and agrochemicals. Its potential as a drug candidate in medicinal chemistry is further highlighted by its pharmacological properties.

80395-16-0

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80395-16-0 Usage

Uses

Used in Organic Synthesis:
Phosphonic acid, [(3-fluorophenyl)methyl]is utilized as a key intermediate in organic synthesis for the preparation of various compounds. Its unique structure and reactivity facilitate the formation of complex molecules and contribute to the advancement of chemical research and development.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Phosphonic acid, [(3-fluorophenyl)methyl]serves as a building block for the synthesis of new drugs. Its incorporation into drug molecules can enhance their efficacy, selectivity, and pharmacokinetic properties, leading to the development of innovative therapeutic agents.
Used in Agrochemical Development:
Phosphonic acid, [(3-fluorophenyl)methyl]is also employed in the agrochemical sector for the creation of novel compounds with potential applications in crop protection and pest control. Its unique properties can contribute to the design of more effective and environmentally friendly agrochemicals.
Used in Medicinal Chemistry Research:
As a potential drug candidate, Phosphonic acid, [(3-fluorophenyl)methyl]is explored in medicinal chemistry for its pharmacological properties. Its unique structure may offer new avenues for the treatment of various diseases and conditions, making it a promising area of research in drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 80395-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80395-16:
(7*8)+(6*0)+(5*3)+(4*9)+(3*5)+(2*1)+(1*6)=130
130 % 10 = 0
So 80395-16-0 is a valid CAS Registry Number.

80395-16-0 Well-known Company Product Price

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  • Aldrich

  • (795593)  3-Fluorobenzylphosphonic acid  

  • 80395-16-0

  • 795593-250MG

  • 848.25CNY

  • Detail

80395-16-0Downstream Products

80395-16-0Relevant academic research and scientific papers

The mode of substrate-recognition mechanism of arylmalonate decarboxylase

Kawasaki, Takayasu,Saito, Koji,Ohta, Hiromichi

, p. 351 - 352 (1997)

A mode of substrate-recognition mechanism by an enzyme, arylmalonate decarboxylase, is proposed. 19F-and 31P-NMR spectra of a complex consisting of the enzyme and an active site-directed inhibitor demonstrated that a hydrophobic interaction between the enzyme and its substrate via their aromatic rings was especially important for the enzyme function.

ORGANOSULPHUR PHOSPHORUS ACID COMPOUNDS. PART 4. FLUOROBENZYLPHOSPHONO-SULPHONIC ACIDS

Montoneri, E.,Savarino, P.,Viscardi, G.,Gallazzi, M. C.

, p. 145 - 156 (2007/10/02)

Four new organosulphur phosphorus acid compounds have been obtained by sulphonation with liquid SO3: 2-fluorobenzylphosphonic and 4-fluorobenzylphosphonic acids gave 2-fluorobenzylphosphono-5-sulphonic and 4-fluorobenzylphosphono-3-sulphonic acids respectively, in nearly quantitative yields; 3-fluorobenzylphosphonic acid gave 3-fluorobenzylphosphono-6-sulphonic acid (85percent) and 3-fluorobenzylphosphono-4-sulphonic acid (15percent).Product structures are based on 13C magnetic resonance data.The entry of the SO3H group into the aromatic ring seems mainly ruled by the fluorinesubstituent.Key words: Sulphonation; fluorobenzylphosphonic acid; fluorobenzylphosphono-sulphonic acid.

Method of increasing the yields of sugar cane with phosphonic acids

-

, (2008/06/13)

This invention discloses a method of increasing the recoverable sugar contained in sugar cane which comprises contacting the sugar cane plant with an effective amount of a compound of the formula STR1 wherein X is selected from the group consisting of alkyl, halogen, trifluoromethyl and alkoxy; n is an integer from 0 to 5; and Z is a straight or branched alkylene group containing from 1 to 5 carbon atoms.

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