22086-45-9 Usage
Uses
Used in Pharmaceutical Synthesis:
9-BROMO-9-BORABICYCLO[3.3.1]NONANE is used as a key reagent in the synthesis of pharmaceuticals for its ability to efficiently functionalize carbon-carbon multiple bonds. This property is crucial in creating complex molecular structures required for new drug development.
Used in Agrochemical Synthesis:
In the agrochemical industry, 9-BROMO-9-BORABICYCLO[3.3.1]NONANE is utilized as a selective reducing agent for the synthesis of various agrochemicals, contributing to the development of effective and targeted pest control agents.
Used in Fine Chemicals Synthesis:
9-BROMO-9-BORABICYCLO[3.3.1]NONANE is employed as a versatile reagent in the synthesis of fine chemicals, where its mild and highly regioselective reduction reactions are advantageous for producing high-purity specialty chemicals used in various industries.
Used in Organic Chemistry Research:
As a valuable tool in organic chemistry, 9-BROMO-9-BORABICYCLO[3.3.1]NONANE is used in research settings to explore novel reduction reactions and develop new synthetic methodologies, further expanding the scope of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 22086-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22086-45:
(7*2)+(6*2)+(5*0)+(4*8)+(3*6)+(2*4)+(1*5)=89
89 % 10 = 9
So 22086-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14BBr/c10-9-7-3-1-4-8(9)6-2-5-7/h7-8H,1-6H2
22086-45-9Relevant academic research and scientific papers
1,5-Cyclooctanediylboryl Selenides - Preparation, Characterisation, and Application
Koester, Roland,Seidel, Guenter,Yalpani, Mohamed
, p. 1815 - 1824 (2007/10/02)
Bis(1,5-cyclooctanediylboryl) selenide (C8H14B)2Se (1) is obtained quantitatively from bis(9-borabicyclononane) (9-BBN)2 and elemental selenium in mesitylene at 150 deg C accompanied by evolution of hydrogen.Bis(1,5-cyclooctanediylboryl) diselenide (C8H14BSe)2 (2) is prepared efficiently from 1 with selenium in mesitylene at 120 deg C. 9-(Hydroseleno)-9-BBN (1H) together with 9-(phenylamino)-9-BBN (3) is easily obtained from 1 and aniline. - γ-Picoline (γPic) reacts with 1 to give the 2:1 addition compound γPic2-1, trimethylphosphane (TMP) with 1 forms the 1:1 addition compound TMP-1.Selenide 1 reacts spontaneously at room temperature with trialkoxyboranes B(OR)3 or with ClnAl(C2H5)3-n compounds exchanging the substituents. - The 1:1 addition compounds γPic-1H, TMP-1H, and Q-1H, are prepared from 1H with γPic, TMP, and quinuclidin (Q), respectively. - 1, 1H, and 2 undergo Se/O exchange reactions with organic and other oxygenated compounds and add to certain CC triple bonds.Pure Fe2Se3 is prepared quantitatively from 1 and Fe2O3. - Key Words: Boryl selenides, 1,5-cyclooctanediyl- / 9-Borabicyclononane, 9-hydroseleno- / Selenidation reagents / Lewis base - organoboron selenium compounds / Borane exchange reactions
