25741-84-8 Usage
Uses
Used in Organic Synthesis:
(N,N-dimethylmethanamine)(hydrido)diiodoboron is used as a reagent in organic synthesis for its ability to facilitate the transfer of hydride ions in chemical reactions. This property makes it a valuable tool in the formation of various organic molecules, contributing to the development of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (N,N-dimethylmethanamine)(hydrido)diiodoboron is used as a catalyst to expedite specific chemical reactions, which can lead to the synthesis of pharmaceutical compounds. Its versatility in participating in reactions involving boron and iodine groups makes it a preferred choice for certain types of reactions in drug development.
Used in Chemical Research:
(N,N-dimethylmethanamine)(hydrido)diiodoboron is also utilized in chemical research as a model compound to study the behavior of hydride ions and the reactivity of boron and iodine groups. This helps researchers understand the underlying mechanisms of various chemical reactions and develop new strategies for synthesizing complex organic molecules.
Overall, (N,N-dimethylmethanamine)(hydrido)diiodoboron is a multifaceted compound with a range of applications in organic chemistry, pharmaceuticals, and chemical research, making it an essential component in the development of new organic molecules and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 25741-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,4 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25741-84:
(7*2)+(6*5)+(5*7)+(4*4)+(3*1)+(2*8)+(1*4)=118
118 % 10 = 8
So 25741-84-8 is a valid CAS Registry Number.
25741-84-8Relevant academic research and scientific papers
The kinetics and mechanism of trimethylamine-haloborane hydrolysis
Lowe, John R.,Uppal, Surjit S.,Weidig, Charles,Kelly, Henry C.
, p. 1423 - 1427 (2008/10/08)
The rates of solvolysis of trimethylamine-monohaloboranes in aqueous dioxane at 25° increase in the series (CH3)3NBH2Cl 3)3NBH2Br 3)3NBH2I. The diiodoborane adduct reacts more slowly than the monoiodo compound but faster than trimethylamine-borane. Only a very slight retardation in rate is observed on substitution of deuterium for hydrogen on boron in the diiodo derivative (kH/kD = 1.1); however, a noticeable solvent isotope effect (kH2O/kD2O = 1.8) is observed for hydrolysis of both the mono- and diiodoborane adducts in 67% aqueous dioxane at 25°. Rates increase with increasing water content of the aqueous dioxane solvent system. No significant effect on rate of acidity is seen for hydrogen ion concentrations as high as 0.3 M or hydroxide ion concentrations up to 0.1 M, nor is the rate appreciably affected by the addition of potassium chloride or potassium iodide up to 0.3 M. The results indicate a mechanism for hydrolysis of the halo compounds quite different from that postulated for amine-BH3 adducts. It is proposed that a rate-determining cleavage of a boron-halogen bond is followed by rapid collapse of an incipient boron(1+) ion. An analogy to nucleophilic substitution reactions in haloborane-amines leading to kinetically stable boronium ions is suggested.
