16523-54-9 | Dicyclohexylchlorophosphine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$15.00	$10.00
5g	98%	in stock	$38.00	$26.00
25g	98%	in stock	$90.00	$63.00
50g	98%	in stock	$170.00	$119.00
100g	98%	in stock	$322.00	$225.00

Description

• Catalog Number: AA87926
• Chemical Name: Dicyclohexylchlorophosphine
• CAS Number: 16523-54-9
• Molecular Formula: C12H22ClP
• Molecular Weight: 232.7298
• MDL Number: MFCD00014294
• SMILES: ClP(C1CCCCC1)C1CCCCC1

Computed Properties

• Complexity: 142
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Rotatable Bond Count: 2
• XLogP3: 4.3

Upstream Synthesis Route

Dicyclohexylchlorophosphine, commonly known as DCCP, is a versatile chemical reagent that finds widespread application in chemical synthesis. As a phosphorus-based compound, DCCP serves as a valuable building block in organic chemistry, particularly in the formation of carbon-phosphorus bonds.In chemical synthesis, DCCP is commonly employed as a phosphination agent, facilitating the introduction of phosphorus-containing functional groups into organic molecules. Its reactivity lies in its ability to undergo nucleophilic substitution reactions, where the chlorine atom is substituted with various nucleophiles, leading to the formation of new carbon-phosphorus bonds. This characteristic makes DCCP a valuable tool in the synthesis of phosphine ligands, organophosphorus compounds, and phosphorus-containing heterocycles.Furthermore, DCCP is utilized in the preparation of phosphorus-based catalysts and reagents, which play a crucial role in numerous organic transformations and industrial processes. Its compatibility with a wide range of functional groups and its high reactivity under mild reaction conditions make DCCP a preferred choice for chemists working on complex organic synthesis projects.Overall, Dicyclohexylchlorophosphine serves as a versatile and indispensable reagent in modern chemical synthesis, enabling the efficient construction of diverse organic molecules with phosphorus functionalities.

Literature

• Ambident PCN heterocycles: N- and P-phosphanylation of lithium 1,3-benzazaphospholides.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20091116