15873-72-0

Usage

Uses

Used in Pharmaceutical Industry:
Dicyclohexylphosphinyl chloride is utilized as a coupling reagent for the synthesis of amides and esters, playing a pivotal role in the production of peptides and other complex organic molecules. Its ability to react with carboxylic acids and amino groups to form amide bonds is crucial for the creation of these biologically significant compounds.
Used in Polymer Production:
In the polymer industry, DCC is employed as a stabilizer, contributing to the production of certain polymers by enhancing their stability and performance characteristics.
Used in Organic Chemistry:
Dicyclohexylphosphinyl chloride also functions as a catalyst in organic chemistry, specifically for addition and elimination reactions. This dual role as both a reagent and a catalyst underscores its importance in facilitating a variety of chemical transformations.

Upstream product

• 931-51-1 cyclohexylmagnesiumchloride 
• 110-82-7 cyclohexane 
• 1005-22-7 cyclohexylphosphonic dichloride 
• 14717-29-4 dicyclohexylphosphine oxide 
• 832-39-3 dicyclohexylphosphinic acid 

Downstream Products

• 832-39-3 dicyclohexylphosphinic acid 
• 67471-61-8 C₁₂H₂₂Cl₃P 
• 2751-99-7 Hydrazin-mono(dicyclohexylphosphinoxid) 
• 101676-23-7 Dicyclohexyl-phosphinsaeure-cyclohexylester 
• 123790-92-1 2,2'-bis(dicyclohexylphosphine dioxide)-6,6'-dimethyl-1,1'-biphenyl 
• 944555-17-3 1-(dicyclohexylphosphinoylethynyl)-2-methoxynaphthalene 
• 1334054-14-6 [cHex₂P(=O)NC₅H₄-4-OCH₃]+Cl- 
• 20412-07-1 C₆H₅⁽²⁾H₂N*Cl⁽²⁾H 
• 39274-83-4 C₇H₇⁽²⁾H₂N*Cl⁽²⁾H 
• 39274-84-5 C₆H₄⁽²⁾H₂ClN*Cl⁽²⁾H 

Relevant academic research and scientific papers

Effect of anomalous aryl strengthening in the series of N-phosphorylureas

Within the series of model N-diorganophosphoryl-N′-n-octylureas, the ability to extract uranium(VI) from nitric acid solutions is maximal for N-diphenylphosphoryl derivative and sharply decreases when phenyl groups are replaced with n-alkyl or cycloalkyl

Preparation of 3-substituted cephalosporins

There is described a process for preparing an enamine of formula (IX): STR1 where R2 is a carboxylic acid protecting group and R3 is the residue of a carboxylic acid derived acyl group and where R5 and R6 are the same or different C1-4 alkyl or C7-10 aralkyl groups; or taken together with the adjacent nitrogen atom form a heterocyclic ring containing from 4 to 8 carbon atoms and optionally a further heteroatom selected from oxygen and nitrogen; by reacting a compound of formula (XII): STR2 with an amine of formula HNR5 R6, the reactant of formula (XII) being prepared by reaction of an appropriate enol derivative with a phosphorus reagent. The enamines of formula (IX) are useful in the preparation of 3-hydroxycephalosporins.