13396-80-0 Usage
Uses
Used in Organic Synthesis:
9-Phosphabicyclo[4.2.1]nonane is used as a building block in organic synthesis for its unique reactivity and structural properties, enabling the creation of novel compounds and molecules with specific functionalities.
Used in Material Science:
In the field of material science, 9-Phosphabicyclo[4.2.1]nonane is utilized as a component in the development of new materials with enhanced properties, such as improved stability, reactivity, or selectivity.
Used as a Ligand in Coordination Chemistry:
9-Phosphabicyclo[4.2.1]nonane is employed as a ligand in coordination chemistry, where it can form complexes with metal ions, contributing to the properties and reactivity of the resulting coordination compounds.
Used in Catalysis:
As a catalyst or catalyst precursor, 9-Phosphabicyclo[4.2.1]nonane is used in various chemical reactions to improve reaction rates, selectivity, and efficiency, making it a valuable tool in the development of green and sustainable chemical processes.
Used in Chemical and Industrial Processes:
9-Phosphabicyclo[4.2.1]nonane is utilized in a wide range of chemical and industrial processes, where its unique properties can be harnessed to improve process efficiency, product quality, or to enable new types of reactions and transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 13396-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13396-80:
(7*1)+(6*3)+(5*3)+(4*9)+(3*6)+(2*8)+(1*0)=110
110 % 10 = 0
So 13396-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H15P/c1-2-4-8-6-5-7(3-1)9-8/h7-9H,1-6H2
13396-80-0Relevant academic research and scientific papers
Downing, Joanne H.,Gee, Victoria,Pringle, Paul G.
, p. 1527 - 1528 (1997)
The isomeric [3.3.1]- and [4.2.1]-phosphabicyclononanes are readily separated by a sequence of hydrophosphination/ dehydrophosphination steps; new diphosphine ligands derived from the [3.3.1] isomer are described.
BISPHOSPHONIUM SALT AND PROCESS FOR PRODUCING THE SAME
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Page 6, (2010/02/07)
A bis-phosphonium salt represented by the following formula (1) is provided: wherein R1, R2, R3, and R4 each represent a linear or branched alkyl group, a cycloalkyl group, an aryl group, or an aralkyl group; A represents an alkylene group; Y represents an anion; R1 and R2 may form a ring; R3 and R4 may form a ring; and R1, R2, R3, and R4 may be the same or different. A process for producing such a bis-phosphonium salt includes a step of allowing a first secondary phosphine and second secondary phosphine to react with a compound in an alcohol solvent selected from a secondary alcohol and tertiary alcohol. The compound is represented by the following formula (5): Y—A—Y??(5)
