6166-10-5 Usage
Boron-containing organic compound
A compound that includes a boron atom bonded to carbon atoms, as well as other elements like hydrogen and oxygen.
Structure
A boron atom bonded to three hydrogen atoms and a methoxy group (CH3O-), forming a stable structure.
Use as a reagent
1-methoxyborolane is commonly used in organic synthesis to facilitate chemical reactions and produce desired products.
Boron source
The compound serves as a source of boron in the preparation of various boron-containing compounds.
Catalytic properties
1-methoxyborolane acts as a catalyst in several chemical reactions, such as hydrosilylation of alkenes and reduction of organic compounds.
Potential medical application
1-methoxyborolane has been investigated for its possible use in boron neutron capture therapy for cancer treatment, due to its boron-10 content.
Selective accumulation
The boron-10 content in 1-methoxyborolane allows it to selectively accumulate in tumor cells, making it a potential candidate for targeted cancer therapy.
Versatility
1-methoxyborolane has a wide range of applications in both chemical synthesis and medical research, showcasing its adaptability and usefulness.
Check Digit Verification of cas no
The CAS Registry Mumber 6166-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6166-10:
(6*6)+(5*1)+(4*6)+(3*6)+(2*1)+(1*0)=85
85 % 10 = 5
So 6166-10-5 is a valid CAS Registry Number.
6166-10-5Relevant academic research and scientific papers
Chiral borane reagents
-
, (2008/06/13)
Chiral borane reagents and their organosilicon derivatives are disclosed.
Boron Compounds, LIV. 17O NMR Studies of Cyclic Organo-Boron-Oxygen Compounds
Wrackmeyer, Bernd,Koester, Roland
, p. 2022 - 2034 (2007/10/02)
17O-Chemical shifts (?17O) of various cyclic organo-boron-oxygen compounds (borolanes, borinanes, 9-borabicyclononanes, boroxins) are reported (Table 1).The ?17O values show that the magnetic screening of oxygen depends upon BO(pp)?-bonds.The contribution of the paramagnetic term ?(p) to the screening (?) of oxygen is evident from the comparison of ?17O of linear and bent systems, as is true for ?14N values of comparable compounds.Differences between 2-ethyl-1,3,2-dioxaborolanes and 2-ethyl-1,3,2-dioxaborinanes are shown by comparison of the ?17O data of the methyl substituted derivatives.
