2175-86-2 Usage
Description
(4-NITRO-PHENYL)-PHOSPHONIC ACID, with the molecular formula C6H6NO6P, is a phosphonic acid derivative featuring a nitrophenyl group attached to the phosphorus atom. (4-NITRO-PHENYL)-PHOSPHONIC ACID is known for its unique chemical properties and serves as a versatile intermediate in the synthesis of a variety of organic compounds.
Uses
Used in Pharmaceutical Industry:
(4-NITRO-PHENYL)-PHOSPHONIC ACID is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure allows it to be a building block for creating new drugs with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, (4-NITRO-PHENYL)-PHOSPHONIC ACID is utilized as a reagent in chemical reactions to produce agrochemicals. Its role in the synthesis of various compounds makes it a valuable asset in developing new pesticides or other agricultural products.
Used as a Reagent in Chemical Reactions:
(4-NITRO-PHENYL)-PHOSPHONIC ACID is employed as a reagent in various chemical reactions, facilitating the synthesis of a wide range of organic compounds for different applications across various industries.
Safety Precautions:
It is crucial to handle (4-NITRO-PHENYL)-PHOSPHONIC ACID with care, as it may pose risks if ingested or comes into contact with the skin or eyes. Proper safety measures should be taken to minimize potential harm during its use and manipulation.
Check Digit Verification of cas no
The CAS Registry Mumber 2175-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2175-86:
(6*2)+(5*1)+(4*7)+(3*5)+(2*8)+(1*6)=82
82 % 10 = 2
So 2175-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6NO5P/c8-7(9)5-1-3-6(4-2-5)13(10,11)12/h1-4H,(H2,10,11,12)
2175-86-2Relevant articles and documents
ETUDE D'UN SCHEMA DE SYNTHESE PEPTIDIQUE INTRAMOLECULAIRE A L'AIDE DE DERIVES DU PHOSPHORE TETRAEDRIQUE
Mulliez, M.
, p. 2027 - 2041 (2007/10/02)
A new scheme of repetitive and controlled peptide synthesis offers two advantages compared to the usual methods of synthesis: two steps only are used for the prolongation of a peptide chain with an amino-acid residue and the risk of racemisation is minimized.The two postulated steps are verified particularly by the rearrangement, in an alkaline alcoholic medium, of phosphordiamides 1 incorporating one amino-acid residue, leading to the formation of the peptide derivatives 6 and 8.The severe limitations of this method are discussed.
