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(R,S)-Diisopropyl hydroxy(2-nitrophenyl)methylphosphonate is a complex organic compound with the molecular formula C12H18NO5P. It is a chiral molecule, meaning it has two enantiomers (R and S) that are mirror images of each other. (R,S)-Diisopropyl hydroxy(2-nitrophenyl)methylphosphonate is characterized by its phosphonate group, which is a key structural feature, and a 2-nitrophenyl group, which introduces a nitro functional group. The compound is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals, due to its potential applications as a chiral building block or a reagent in asymmetric synthesis. It is also known for its potential use in the development of new materials and as a research tool in studying the properties of chiral molecules.

96181-15-6

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96181-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96181-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,8 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96181-15:
(7*9)+(6*6)+(5*1)+(4*8)+(3*1)+(2*1)+(1*5)=146
146 % 10 = 6
So 96181-15-6 is a valid CAS Registry Number.

96181-15-6Relevant academic research and scientific papers

Unsymmetrical dimethylhydrazine in phosphorylation reactions

Ryapisova

, p. 1533 - 1535 (2007/10/03)

The reaction of dialkyl hydrogen phosphites with nitrobenzaldehyde dimethylhydrazone leads to formation of compounds having a salt-like structure, while the reaction with hydrazones gives phosphonates. α-Dimethylhydrazinophosphonates were obtained by the

Asymmetric Synthesis of Chiral, Nonracemic Dialkyl α-Hydroxyarylmethyl- and α-, β- and γ-Hydroxyalkylphosphonates from Keto Phosphonates

Meier, Chris,Laux, Wolfgang H. G.,Bats, Jan W.

, p. 1963 - 1980 (2007/10/03)

The enantioselective synthesis of α-hydroxyarylmethylphosphonates 2a-p by the oxazaborolidine-catalyzed reduction of α-keto phosphonates 1a-p using different boranes 4a-c was studied in detail.Moderate to good enantioselectivities are found (up to 80perce

ASYMMERIC CATALYSIS IN CARBON-PHOSPHORUS BOND FORMATION

Wynberg, Hans,Smaardijk, Ab A.

, p. 5899 - 5900 (2007/10/02)

o-Nitrobenzaldehyde reacts smoothly with dialkylphosphonates in the presence of catalytic quantities of cinchona alkaloids (e.g.quinine) to produce the α-hydroxy phosphonate esters in excellent chemical yields, with excellent enantiomeric enrichment.

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