1499-22-5

Basic information

• Product Name: ETHYL PHENYL PHOSPHINSAEURECHLORID
• Synonyms: ETHYL PHENYL PHOSPHINSAEURECHLORID
• CAS NO: 1499-22-5
• Molecular Formula: C₈H₁₀ClOP
• Molecular Weight: 188.591161
• Mol File: 1499-22-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ETHYL PHENYL PHOSPHINSAEURECHLORID(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL PHENYL PHOSPHINSAEURECHLORID(1499-22-5)
• EPA Substance Registry System: ETHYL PHENYL PHOSPHINSAEURECHLORID(1499-22-5)

Safety Data

• Hazardous Substances Data: 1499-22-5(Hazardous Substances Data)

Upstream product

• 1638-86-4 diethyl phenylphosphonite 
• 75-03-6 ethyl iodide 
• 644-97-3 Dichlorophenylphosphine 
• 6829-76-1 ethylphenylphosphinic acid methyl ester 
• 6587-98-0 ethyl ester of ethylphenylthiophosphinic acid 
• 76-03-9 trichloroacetic acid 
• 15849-83-9 ethylphenylphosphinous chloride 
• 79-43-6 dichloro-acetic acid 
• 2227-43-2 ethylphenylphosphinic acid ethyl ester 
• 13317-44-7 ethyl(phenyl)phosphinic acid 

Downstream Products

• 85656-04-8 ethylphenylphosphinic azide 
• 114187-99-4 Aethyl-phenyl-thiopyrophosphinat 
• 883857-25-8 C₂₆H₃₇O₇P 
• 883857-04-3 C₂₆H₃₇O₇P 
• 918660-73-8 4-acetylphenyl ethyl(phenyl)phosphinate 
• 13317-44-7 ethyl(phenyl)phosphinic acid 
• 2227-43-2 ethylphenylphosphinic acid ethyl ester 
• 1499-23-6 -amidophosphonsaeure-diaethylester 
• 72974-38-0 dicyclohexylammonium (-)-(S)-ethylphenylphosphinothioate 
• 101522-96-7 dicyclohexylammonium ethylphenylphosphinothioate 
• 57322-10-8 (-)-(S)-S-methyl ethylphenylphosphinothioate 
• 76420-34-3 S-methyl ethylphenylphosphinothioate 
• 85656-07-1 methyl N-phenyl-P-ethylphosphonamidate 
• 94193-60-9 N-(ethylphenylphosphinoyl)-O-methanesulphonylhydroxylamine 

Relevant articles and documents

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Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands

A practical synthesis of optically pure alkylphenylvinylphosphine oxides is described, utilizing a nucleophilic displacement at phosphorus to install the vinyl moiety. The products were used to prepare classes of P-stereogenic aminophosphine (PN) and aminohydroxyphosphine (PNO) ligands. Stereocontrol can be exerted at various stages of the synthesis, to provide specific combinations of chirality in the final product. The effect of the stereogenic phosphorus and match-mismatch of chiralities of PNO ligands were examined in the asymmetric ruthenium-catalyzed hydrogen transfer reduction of three aryl ketones.

Enantiomerically pure zinc phosphonates based on mixed phosphonic acid - Phosphine oxide chiral building blocks

The coordination chemistry of enantiomerically pure phosphonic acids H2O3PCH2P(O)(C6H5)(R) [R = CH3 and C2H5] with zinc is described. The structures of two new optical