1530-35-4

Usage

Uses

Used in Pharmaceutical Production:
CINNAMYLTRIPHENYLPHOSPHONIUM CHLORIDE is used as a phase transfer catalyst for the synthesis of various pharmaceuticals. It aids in the efficient production of complex organic compounds, enhancing the overall manufacturing process.
Used in Agrochemical Production:
In the agrochemical industry, CINNAMYLTRIPHENYLPHOSPHONIUM CHLORIDE is employed as a phase transfer catalyst to facilitate the synthesis of active ingredients for pesticides and other agricultural chemicals. This results in improved control over the reactions and increased yields.
Used in Fine Chemicals Production:
CINNAMYLTRIPHENYLPHOSPHONIUM CHLORIDE is used as a phase transfer catalyst in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, dyes, and other specialty products. Its use allows for greater control and efficiency in the production process.

InChI:InChI=1/C27H24P.ClH/c1-5-14-24(15-6-1)16-13-23-28(25-17-7-2-8-18-25,26-19-9-3-10-20-26)27-21-11-4-12-22-27;/h1-22H,23H2;1H/q+1;/p-1/b16-13+;

Upstream product

• 603-35-0 triphenylphosphine 
• 2687-12-9 cinnamyl chloride 
• 15600-34-7 cinnamyl chloroformate 

Downstream Products

• 34944-28-0 1-(2-nitrophenyl)-4-phenylbutadiene 
• 27331-30-2 1-(3-Chlorphenyl)-4-phenyl-1,3-butadien 
• 864818-50-8 (2E,7E,9E)-10-Phenyl-deca-2,7,9-trienoic acid methyl ester 
• 114444-89-2 [(1E,3E)-4-cyclohexylbuta-1,3-dien-1-yl]benzene 
• 1222087-99-1 (8E)-1,9-diphenylnona-6,8-dien-1-one 
• 7354-48-5 2-(4-phenyl-buta-1,3-dienyl)-pyrrole 
• 89346-87-2 2-(4-phenylbutyl)benzenediazonium tetrafluoroborate 
• 76691-98-0 1-(2-aminophenyl)-4-phenylbutane 
• 85479-36-3 4,5α-epoxy-7α-(hydroxymethyl)-3-methoxy-17-methyl-7β-(4-phenyl-1,3-butadienyl)morphinan-6β-ol 
• 85455-23-8 4,5α-epoxy-7α-(hydroxymethyl)-3-methoxy-17-methyl-7β-(4-phenylbutyl)morphinan-6β-ol 
• 85455-24-9 4,5α-epoxy-7α-(hydroxymethyl)-17-methyl-7β-(4-phenylbutyl)morphinan-3,6β-diol 
• 90281-04-2 t-2R*-(1',1'-dichloro-t-3'-phenylcycloprop-r-2'R*-yl)-r-3-(2,6-dichlorophenyl)oxirane 
• 90281-03-1 threo-t-3-phenyl-c-3'-(2,6-dichlorophenyl)-2,2'-bioxiranyl 
• 90281-03-1 erythro-t-3-phenyl-t-3'-(2,6-dichlorophenyl)-2,2'-bi-oxiranyl 

Relevant academic research and scientific papers

Synthesis of aryl and heterocyclic polyenes and their activity in free radical scavenging

Aryl polyenes and heterocyclic polyenes with the same central C20 unit of β,β-carotene but different terminal groups were synthesised. Their free radical scavenging activity was measured by a 1,1-diphenyl-2-picrylhydrazinyl spectrophotometric method. The results indicated that all the new compounds have free radical scavenging activity.

Phase-Transfer-Catalyzed Gomberg-Bachmann Synthesis of Unsymmetrical Biarenes: A Survey of Catalysts and Substrates

Two problems have hindered the Gomberg-Bachmann (GB) and Pschorr reactions of arenediazonium cations: the instability of the arenediazonium salts and side reactions.Arenediazonium tetrafluoroborate and hexafluorophosphate salts can be prepared in high yield and purity and can be stored safely.Unfortunately, these salts are insoluble in most nonpolar organic solvents.Crown ether complexation or other phase-transfer (pt) catalytic methodology can ameliorate this situation, and reactions conducted by the approaches outlined herein often afforded coupling or cyclization products in high yield and corresponding purity.The use of crown ethers, quarternary 'onium salts, lipophilic carboxylic acid salts, and even the polar cosolvent acetonitrile increase the utility of the ptGB reaction dramatically.Sixty examples of couplings are reported along with an assessment of selectivities.A number of examples are also presented of phase-transfer-type Pschorr cyclizations.In the latter case, the use of potassium superoxide, KO2, is introduced to suppress indazole formation.