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9-Phosphabicyclononanes, a class of organic compounds, are characterized by their bicyclic ring system that incorporates a phosphorus atom. They have garnered attention for their potential as ligands in coordination chemistry and as precursors to organophosphorus compounds. Their applications span across catalysis, materials science, and the synthesis of biologically active molecules, making them promising building blocks for the development of new pharmaceuticals and agrochemicals.

13887-02-0

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13887-02-0 Usage

Uses

Used in Coordination Chemistry:
9-Phosphabicyclononanes serve as versatile ligands, enhancing the properties of metal complexes and facilitating various chemical reactions.
Used in Organophosphorus Compounds Synthesis:
As precursors, these compounds are instrumental in the creation of organophosphorus compounds, which are essential in a variety of chemical applications.
Used in Catalysis:
9-Phosphabicyclononanes are utilized in catalytic processes, improving the efficiency and selectivity of chemical reactions.
Used in Materials Science:
These compounds contribute to the development of new materials with unique properties, such as high thermal stability and specific reactivity.
Used in the Synthesis of Biologically Active Molecules:
9-Phosphabicyclononanes are employed as intermediates in the synthesis of biologically active molecules, potentially leading to new pharmaceuticals and agrochemicals.
Used in Pharmaceutical Development:
As building blocks, 9-phosphabicyclononanes are crucial in the design and synthesis of novel pharmaceuticals, targeting a wide range of therapeutic areas.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, these compounds are used to develop new pesticides and other crop protection agents, enhancing agricultural productivity and sustainability.

Check Digit Verification of cas no

The CAS Registry Mumber 13887-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13887-02:
(7*1)+(6*3)+(5*8)+(4*8)+(3*7)+(2*0)+(1*2)=120
120 % 10 = 0
So 13887-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H15P/c1-3-7-5-2-6-8(4-1)9-7/h7-9H,1-6H2

13887-02-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-phosphabicyclo[3.3.1]nonane

1.2 Other means of identification

Product number -
Other names Phoban

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13887-02-0 SDS

13887-02-0Relevant academic research and scientific papers

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)

A simple procedure for the separation of the catalytically important phosphabicyclononane isomers

Downing, Joanne H.,Gee, Victoria,Pringle, Paul G.

, p. 1527 - 1528 (2007/10/03)

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.

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