53820-05-6 Usage
Uses
Used in Organic Synthesis:
N-bis(benzylamino)phosphinothioyl-1-phenyl-methanamine is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new organic compounds.
Used in Coordination Chemistry as a Ligand:
In coordination chemistry, N-bis(benzylamino)phosphinothioyl-1-phenyl-methanamine is used as a ligand to form stable complexes with transition metals. Its complexation properties are valuable for studying and developing new coordination compounds with specific properties and applications.
Used in Catalysis:
Due to its capacity to form stable complexes with transition metals, N-bis(benzylamino)phosphinothioyl-1-phenyl-methanamine is used as a catalyst or a catalyst precursor in various chemical processes. Its use in catalysis can enhance the efficiency and selectivity of reactions.
Used in Materials Science:
N-bis(benzylamino)phosphinothioyl-1-phenyl-methanamine has potential applications in materials science, where its complexation ability can be utilized to develop new materials with tailored properties for specific uses.
Used in Pharmaceutical Research:
Given its complex structure and potential biological activity, N-bis(benzylamino)phosphinothioyl-1-phenyl-methanamine may be studied for possible pharmaceutical applications. Its interaction with biological systems is a subject of ongoing research, which could lead to the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 53820-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,2 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53820-05:
(7*5)+(6*3)+(5*8)+(4*2)+(3*0)+(2*0)+(1*5)=106
106 % 10 = 6
So 53820-05-6 is a valid CAS Registry Number.
53820-05-6Relevant academic research and scientific papers
SYNTHETIC, N.M.R. SPECTROSCOPIC AND X-RAY CRYSTALLOGRAPHIC INVESTIGATIONS ON THE PRODUCTS OF THE REACTIONS OF PHENYL (METHYL) PHOSPHONOTHIOIC DICHLORIDE AND THIOPHOSPHORYL CHLORIDE AND PSCl3 WITH PRIMARY AMINES
Hursthouse, Michael B.,Ibrahim, Ezzeldine H.,Parkes, Harold G.,Shaw, Leyla S.,Shaw, Robert A.,Watkins, David A.
, p. 261 - 266 (2007/10/02)
The syntheses in solution of (i) 2,4-dialkylamino-, (ii) 2,4-dimethyl-, and (iii) 2,4-diphenyl-2,4-dithio-cyclodiphosph(V)azanes, 2 (R' = NHR, Ph, or Me; R = alkyl), derived from thiophosphoryl trichloride, methylphosphonothioic and phenylphosphonothioic dichlorides and primary akylamines are described.N.m.r. spectroscopic properties for these cyclodiphosph(V)azanes and their monomeric precursors, R'P(S)(NHR)2 (R' = NHR, Ph, or Me; R = alkyl), are presented and structural inferences are drawn from this data.The X-ray crystal structure of i>2 is reported.
