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Diaminoposphorylbenzene, also known as diaminophosphinobenzene, is an organic compound with the chemical formula C6H10N2P. It is a derivative of benzene, where two hydrogen atoms are replaced by amino groups (-NH2) and one hydrogen atom is replaced by a phosphoryl group (-P(O)H2). diaminophosphorylbenzene is a versatile building block in the synthesis of various phosphorus-containing organic molecules, such as phosphazenes and other organophosphorus compounds, which have applications in materials science, pharmaceuticals, and agrochemicals. Due to its reactivity and the presence of both amino and phosphoryl groups, diaminophosphorylbenzene can participate in a range of chemical reactions, making it a valuable intermediate in organic synthesis.

4707-88-4

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4707-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4707-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4707-88:
(6*4)+(5*7)+(4*0)+(3*7)+(2*8)+(1*8)=104
104 % 10 = 4
So 4707-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N2OP/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H4,7,8,9)

4707-88-4Relevant academic research and scientific papers

Synthesis and characterization of flame-retardant polyurethane elastomers using phosphorus-containing chain extender

Xu, Wenzong,Li, Wenxiu,Ren, Mingyuan,Yin, Jianguo

, p. 5683 - 5685 (2013)

Phenylphosphonic diamine was synthesized from phenylphosphonic dichloride and characterized by Fourier transform infrared spectroscopy and nuclear magnetic resonance. Then phenylphosphonic diamine was used to prepare a series of phosphorus containing poly

Phosphonamidates are the first phosphorus-based zinc binding motif to show inhibition of β-class carbonic anhydrases from bacteria, fungi, and protozoa

Alissa, Siham A.,Alghulikah, Hanan A.,Alothman, Zeid A.,Osman, Sameh M.,Del Prete, Sonia,Capasso, Clemente,Nocentini, Alessio,Supuran, Claudiu T.

, p. 59 - 64 (2019/11/11)

A primary strategy to combat antimicrobial resistance is the identification of novel therapeutic targets and anti-infectives with alternative mechanisms of action. The inhibition of the metalloenzymes carbonic anhydrases (CAs, EC 4.2.1.1) from pathogens (

Phosphorus versus Sulfur: Discovery of Benzenephosphonamidates as Versatile Sulfonamide-Mimic Chemotypes Acting as Carbonic Anhydrase Inhibitors

Nocentini, Alessio,Gratteri, Paola,Supuran, Claudiu T.

supporting information, p. 1188 - 1192 (2019/01/04)

The first zinc-binding group (ZBG) to have been identified as inhibitor of the metallo-enzymes carbonic anhydrases (CA, EC 4.2.1.1) was the sulfonamide. From then on several classes of zinc-binders have been described. This work reports the benzenephospon

The reaction of ammonia-chloramine mixtures with phosphorus-phosphorus bonds

Frazier, Stephen E.,Sisler, Harry H.

, p. 925 - 928 (2007/10/05)

The reactions of ammonia-chloramine mixtures with tetramethyldiphosphine, tetraethyldiphosphine, tetraphenyldiphosphine, and tetraphenylcyclotetraphosphine have been shown to result in the fission of the phosphorus-phosphorus bonds and in the formation of the same products as would be expected from the reaction of ammonia-chloramine mixtures with the corresponding mono- or dihalophosphines. The previously postulated but not isolated compounds [(C6H5)2P(NH2)2]Cl and [(C6H5)P(NH2)3]Cl were obtained. It is postulated that the initial products of the P-P bond fission are R2PCl and R2PNH2. It was also shown that dimethyldiaminophosphonium chloride reacts with PCl5 to yield (CH3)2Cl4P3N3. The mode of formation and the infrared spectrum indicate that this product is a phosphonitrilic cyclic trimer in which both methyl groups are on the same phosphorus atom.

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