936-59-4

Basic information

• Product Name: 3-Chloropropiophenone
• Synonyms: 3-CHLORO-1-PHENYL-1-PROPANONE;3-CHLORO-1-OXO-1-PHENYLPROPANE;B-CHLOROPROPIOPHENONE;BETA-CHLOROPROPIOPHENONE;3-Chloropropiophenone98%;Chloropropiophenone, 98+%;beta-Chloropropiophenone,98+%;3-Chloropropiophenone, tech., 90%
• CAS NO: 936-59-4
• Molecular Formula: C₉H₉ClO
• Molecular Weight: 168.62
• EINECS: 213-317-6
• Product Categories: Ketones;Building Blocks;C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Aromatics, Impurities, Intermediates
• Mol File: 936-59-4.mol
• Article Data: 31

Chemical Properties

• Melting Point: 48-50 °C(lit.)
• Boiling Point: 113-115 °C4 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: faintly yellow to tan crystalline powder
• Density: 1.1115 (rough estimate)
• Refractive Index: 1.5350 (estimate)
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• Water Solubility: Insoluble
• Stability: Stable. Incompatible with strong bases, strong oxidizing agents.
• BRN: 2043580
• CAS DataBase Reference: 3-Chloropropiophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloropropiophenone(936-59-4)
• EPA Substance Registry System: 3-Chloropropiophenone(936-59-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26-24/25
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 936-59-4(Hazardous Substances Data)

Usage

Chemical Properties

faintly yellow to tan crystalline powder

Uses

Different sources of media describe the Uses of 936-59-4 differently. You can refer to the following data:
1. 3-Chloropropiophenone is an Impurity of Fluoxetine (F597100).
2. 3-Chloropropiophenone was used in the asymmetric reduction of (S)-3-chloro-1-phenylpropanol using preheated Candida utilis cells immobilized in calcium alginate gel beads. It was also used in the synthesis of (R)-3-chloro-1-phenyl-1-propanol via asymmetric reduction using in-situ generated oxazaborolidine catalyst derived from (S)-α,α-diphenylprolinol. It is a precursor of phenyl vinyl ketone.

InChI:InChI=1/C9H9ClO/c10-7-6-9(11)8-4-2-1-3-5-8/h1-5H,6-7H2

Synthetic route

2-chloropropionyl chloride (625-36-5) + benzene (71-43-2) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With aluminum (III) chloride In dichloromethane at 0 - 20℃; Inert atmosphere;	100%
aluminium trichloride; nitromethane In carbon disulfide for 2h; Product distribution; Mechanism; Ambient temperature; further Friedel-Crafts catalysts, further arenes, further haloacid chlorides; variation of temperature and time;	88%
aluminium trichloride; nitromethane In carbon disulfide for 2h; Ambient temperature;	88%

phenylpropyl chloride (104-52-9) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With Oxone; potassium bromide In dichloromethane; water at 20℃; for 24h; visible light irradiation;	97%

3-chloro-1-phenyl-propan-1-ol (18776-12-0) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With dihydrogen peroxide; acetic acid; sodium bromide In water at 60℃; for 2h; Inert atmosphere;	93%
With dipotassium peroxodisulfate; V2O5/TiO2 In water; acetonitrile at 80℃; Sealed tube; Green chemistry;	88%
With oxone; C18H17IN2O7PolS(1-)*Na(1+); tetra(n-butyl)ammonium hydrogensulfate In acetonitrile at 70℃; for 18h; Reagent/catalyst; Solvent; Sealed tube; Green chemistry;	84%
With sodium dichromate; sulfuric acid

cinnamyl chloride (2687-12-9) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With iron(II) acetylacetonate; Triethoxysilane In tert-butyl alcohol at 20℃; for 24h; regioselective reaction;	90%
With tris(1-phenylbutane-1,3-dionato)iron(III); phenylsilane In ethanol at 20℃; for 6.5h; Reagent/catalyst; Wacker Oxidation;	81%
With iron(III) chloride; tetraphenylsilane In tert-butyl alcohol at 80℃; for 24h;	90 %Chromat.

Phenyl vinyl ketone (768-03-6) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With Triphenylphosphine oxide In dichloromethane at 20℃; for 2h;	88%
With hydrogenchloride; diethyl ether

1-phenylcyclopropan-1-ol (29526-96-3) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With manganese(II) triflate; tetrabutylammonium acetate; acetic acid; magnesium chloride In acetonitrile at 25℃; for 3.5h; Inert atmosphere; Electrochemical reaction; Sealed tube;	54%

diphenyl cadmium (2674-04-6) + 2-chloropropionyl chloride (625-36-5) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
	51%

diethyl ether (60-29-7) + ethyl 3-chloropropanoate (623-71-2) + phenylmagnesium bromide → 3-chloropropiophenone (936-59-4) + 3,3-diphenylallyl chloride (24626-27-5)

ethyl 3-chloropropanoate (623-71-2) + phenylmagnesium bromide → 3-chloropropiophenone (936-59-4) + 3,3-diphenylallyl chloride (24626-27-5)

Conditions	Yield
With diethyl ether Destillation des nach Hydrolyse erhaltenen Reaktionsprodukts unter vermindertem Druck;

benzoyl chloride (98-88-4) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With ethyl bromide; aluminium trichloride anschliessendes Einleiten von Aethylen;

2-chloropropionyl chloride (625-36-5) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With aluminium trichloride; benzene

hydrogenchloride (7647-01-0) + acetic acid (64-19-7) + 1-phenyl-propan-1-one (93-55-0) → 3-chloropropiophenone (936-59-4) + 2-chloro-1-phenyl-propanone-(1)

Conditions	Yield
an Graphit-Anoden.Electrolysis;

benzene (71-43-2) + β-chloro-propionic acid chloride → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With aluminium trichloride

3-oxo-3-phenylpropyl(triphenyl)bismuthonium tetrafluoroborate → 3-chloropropiophenone (936-59-4) + Phenyl vinyl ketone (768-03-6) + 3-oxo-3-phenylpropyl formate + triphenylbismuthane

Conditions	Yield
With potassium chloride In N,N-dimethyl-formamide for 8h; Ambient temperature;	A 28 % Turnov. B 25 % Turnov. C 25 % Turnov. D n/a

3-chloro-1-phenyl-propan-1-ol (18776-12-0) → 3-chloropropiophenone (936-59-4) + (1R)-3-chloro-1-phenylpropanol (100306-33-0)

Conditions	Yield
With Sphingomonas paucimobilis NCIMB 8195 In water; N,N-dimethyl-formamide for 120h;	A 21 % Chromat. B 79 % Chromat.

formaldehyd (50-00-0) + acetophenone (98-86-2) → 3-chloropropiophenone (936-59-4) + 1-phenyl-3-chloro-2-(chloromethyl)-1-propanone (39192-57-9) + 4-chloromethylacetophenone (54589-56-9) + Phenyl vinyl ketone (768-03-6)

Conditions	Yield
With hydrogenchloride for 2h; Heating; Further byproducts. Title compound not separated from byproducts.;

1-phenyl-propan-1-one (93-55-0) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
With hydrogenchloride; ammonium nitrate; iodine; oxygen In water; acetonitrile at 60℃; for 24h; Green chemistry; regioselective reaction;

benzoic acid ethyl ester (93-89-0) → 3-chloropropiophenone (936-59-4)

Conditions	Yield
Multi-step reaction with 2 steps 1: titanium(IV) isopropylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere; Sealed tube 2: acetic acid; manganese(II) triflate; magnesium chloride; tetrabutylammonium acetate / acetonitrile / 3.5 h / 25 °C / Inert atmosphere; Electrochemical reaction; Sealed tube View Scheme

1,2,3,4-tetrahydroisoquinoline (91-21-4) + 3-chloropropiophenone (936-59-4) → 3-(3,4-dihydro-1H-isoquinolin-2-yl)-1-phenylpropanone (861369-89-3)

Conditions	Yield
With potassium carbonate In acetonitrile at 20℃; for 16h;	100%

6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (1745-07-9) + 3-chloropropiophenone (936-59-4) → 3-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-1-phenyl-propan-1-one (773030-82-3)

Conditions	Yield
With potassium carbonate In acetonitrile at 20℃;	100%

3-chloropropiophenone (936-59-4) + (S)-1-(p-chlorophenyl)ethylamine (4187-56-8) → 3-[(S)-1-(4-chloro-phenyl)-ethylamino]-1-phenyl-propan-1-one (1114563-43-7)

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃;	100%
With triethylamine In tetrahydrofuran at 20℃;

3-chloropropiophenone (936-59-4) → Phenyl vinyl ketone (768-03-6)

Conditions	Yield
With triethylamine In chloroform at 20℃; for 18.0833h; Inert atmosphere;	99%
With triethylamine In chloroform at 0 - 30℃; for 18h;	99%
With triethylamine In chloroform for 18h;	99%

3-chloropropiophenone (936-59-4) → (1R)-3-chloro-1-phenylpropanol (100306-33-0)

Conditions	Yield
With borane; S-oxaborolidine In tetrahydrofuran at 0℃; for 0.833333h;	99%
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; C22H32N4O4S2; water; sodium formate at 40℃; for 0.25h; Air atmosphere; optical yield given as %ee; enantioselective reaction;	99%
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; (1R,2R)-9H-fluorene-2,7-disulfonic acid bis-[(2-amino-cyclohexyl)amide]; sodium formate In water at 40℃; for 0.25h; optical yield given as %ee; enantioselective reaction;	99%

3-chloropropiophenone (936-59-4) + 4-tert-butylphenylboronic acid (123324-71-0) → 3-(4-(tert-butyl)phenyl)-1-phenylpropan-1-one (138722-46-0)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 80℃; under 750.075 Torr; for 30h; Inert atmosphere;	99%

Thien-3-ylboronic acid (6165-69-1) + 3-chloropropiophenone (936-59-4) → 1-phenyl-3-(thiophen-3-yl)propan-1-one (71778-01-3)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	99%

3-chloropropiophenone (936-59-4) → 3-(benzyl(methyl)amino)-1-phenylpropan-1-one (21970-65-0)

Conditions	Yield
	98%

3-chloropropiophenone (936-59-4) + m-tolylboronic acid (17933-03-8) → 1-phenyl-3-(3-methylphenyl)-1-propananone (95465-70-6)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	98%

3-chloropropiophenone (936-59-4) + 1-Naphthylboronic acid (13922-41-3) → 3-(naphthalen-1-yl)-1-phenylpropan-1-one (96550-91-3)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	98%

α-naphthol (90-15-3) + 3-chloropropiophenone (936-59-4) → N,N-dimethylamino-3-(naphthyl-1-oxy)-1-phenylprop-1-amine (119356-76-2)

Conditions	Yield
With sodium hydroxide In N,N-dimethyl-formamide at 60 - 65℃; for 5h; Reagent/catalyst; Temperature;	97.7%

3-chloropropiophenone (936-59-4) → 3-chloro-1-phenyl-propan-1-ol (18776-12-0)

Conditions	Yield
With sodium tetrahydroborate In tetrahydrofuran at 20℃; for 2h;	97%
With sodium tetrahydroborate In methanol at 20℃; for 24h; Inert atmosphere;	95%
With sodium tetrahydroborate; ethanol In tetrahydrofuran at -10 - -5℃; for 0.333333h; Inert atmosphere;	95%

3-chloropropiophenone (936-59-4) + allyl bromide (106-95-6) → 1-chloro-3-phenyl-5-hexen-3-ol (143427-44-5)

Conditions	Yield
With water; ammonium chloride; zinc In tetrahydrofuran Reflux;	97%
With water; ammonium chloride; zinc In tetrahydrofuran Inert atmosphere;	97%
With ammonium chloride; zinc In tetrahydrofuran; water for 1h; Reflux;	97%

3-chloropropiophenone (936-59-4) + phenylboronic acid (98-80-6) → dihydrochalcone (1083-30-3)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Reagent/catalyst; Solvent; Temperature; Concentration; Inert atmosphere;	97%

3-chloropropiophenone (936-59-4) + 4-fluoroboronic acid (1765-93-1) → 1-phenyl-3-(4-fluorophenyl)-1-propananone (41865-46-7)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	97%

α-naphthol (90-15-3) + 3-chloropropiophenone (936-59-4) → 3-(naphthalen-1-yloxy)-1-phenylpropan-1-one (41198-42-9)

Conditions	Yield
With tetrabutylammomium bromide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane; water at 20℃; for 42h; Temperature; Solvent; Large scale;	97%
Stage #1: α-naphthol With potassium hydroxide In N,N-dimethyl-formamide at 0℃; for 2h; Inert atmosphere; Stage #2: 3-chloropropiophenone In N,N-dimethyl-formamide at 50℃; for 30h; Reagent/catalyst; Temperature; Inert atmosphere;	73.52%

3-chloropropiophenone (936-59-4) + tert-butylamine (75-64-9) → 3-(tert-butylamino)-1-phenylpropan-1-one (2679-37-0)

Conditions	Yield
With potassium carbonate In acetonitrile at 20℃;	96%

3-chloropropiophenone (936-59-4) + 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (72824-04-5) → 1-chloro-3-phenyl-5-hexen-3-ol (143427-44-5)

Conditions	Yield
With ethanol; diethylzinc In tetrahydrofuran at 20℃; for 2h; Inert atmosphere;	96%

3-chloropropiophenone (936-59-4) + (4-(2-hydroxyethoxy)phenyl)(phenyl)methanone (14814-17-6) → ospemifene (128607-22-7)

Conditions	Yield
With titanium tetrachloride; zinc In 2-methyltetrahydrofuran at 15 - 50℃; Product distribution / selectivity;	96%
With titanium tetrachloride; zinc In 2-methyltetrahydrofuran at -10 - 80℃; for 5.5h; Inert atmosphere;
With titanium tetrachloride; zinc In tetrahydrofuran McMurry Reaction; Reflux;
With titanium tetrachloride; zinc In tetrahydrofuran for 6h; McMurry Reaction; Reflux; Inert atmosphere;

3-chloropropiophenone (936-59-4) + B-allenyl-1,3,2-dioxaborolane (1314099-29-0) → (S)-(+)-1-chloro-3-phenylhex-5-yn-3-ol (1314099-35-8)

Conditions	Yield
Stage #1: B-allenyl-1,3,2-dioxaborolane With (S)-3,3'-dibromo-1,1'-bi-2-naphthol at 20℃; for 0.0833333h; Inert atmosphere; Neat (no solvent); Stage #2: 3-chloropropiophenone at 72℃; for 0.75h; Inert atmosphere; Neat (no solvent); Microwave irradiation; optical yield given as %ee; enantioselective reaction;	96%

3-chloropropiophenone (936-59-4) + 2-Methylphenylboronic acid (16419-60-6) → 1-phenyl-3-(2-methylphenyl)-1-propananone (84839-91-8)

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	96%

3-chloropropiophenone (936-59-4) + 4-trifluoromethylphenylboronic acid (128796-39-4) → 1-phenyl-3-(4-(trifluoromethyl)phenyl)propan-1-one

Conditions	Yield
With potassium phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In 1,4-dioxane at 60℃; under 750.075 Torr; for 20h; Inert atmosphere;	96%

3-chloropropiophenone (936-59-4) → (S)-1-phenyl-1-propanol (613-87-6)

Conditions	Yield
With formic acid; C30H31ClN2O2RuS; triethylamine at 60℃; for 1.5h; Inert atmosphere; enantioselective reaction;	96%
Multi-step reaction with 2 steps 1: sodium carbonate / water / 72 h / 28 °C / pH 9 2: yeast strain Rhodotorula glutinis H93 / Microbiological reaction View Scheme
Multi-step reaction with 2 steps 1: triethylamine / chloroform / Inert atmosphere 2: [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; Boc-L-alanine(2S)-hydroxypropylamide; lithium chloride; potassium tert-butylate / tetrahydrofuran; ethanol / 40 °C / Inert atmosphere View Scheme

4,4'-Dihydroxybenzophenone (611-99-4) + 3-chloropropiophenone (936-59-4) → 4,4'-(4"-chloro-2"-phenylbut-1"-ene-1",1"-diyl)diphenol

Conditions	Yield
With titanium tetrachloride; zinc In tetrahydrofuran at 0 - 20℃; for 5h; McMurry Reaction; Inert atmosphere; Reflux;	96%
With titanium tetrachloride; zinc In tetrahydrofuran for 2.5h; McMurry Reaction; Inert atmosphere; Reflux;	70%
With titanium tetrachloride; zinc In tetrahydrofuran McMurry Reaction;

3-chloropropiophenone (936-59-4) + triethyl phosphite (122-52-1) → diethyl (3-oxo-3-phenylpropyl)phosphonate (16324-15-5)

Conditions	Yield
for 6h; Heating;	95%
With aluminum oxide for 0.0833333h; Arbuzov rearrangement; microwave irradiation;	90%
at 85 - 100℃; Kinetics; Thermodynamic data; Mechanism; Ea, ΔH(excit.), ΔS(excit.), ΔG(excit.); other substituted 3-chloropropiophenones; other solvents;
With diethylene glycol dimethyl ether

3-chloropropiophenone (936-59-4) → 3-chloro-1-phenylpropan-1-ol

Conditions	Yield
With sodium tetrahydroborate; dimethyl sulfate; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole In tetrahydrofuran at 0℃; for 1.5h; Inert atmosphere; enantioselective reaction;	95%
2-[(1,3,2-dioxaborolan-2-yloxy)diphenylmethyl]pyrrolidine Product distribution / selectivity;	86%

3-chloropropiophenone (936-59-4) + B-allyl-1,3,2-dioxaborinane (54655-41-3) → (R)-(-)-1-chloro-3-phenylhex-5-en-3-ol

Conditions	Yield
With (S)-3,3'-dibromo-1,1'-bi-2-naphthol; tert-butyl alcohol at 20℃; for 24h; Inert atmosphere; enantioselective reaction;	95%

3-chloropropiophenone (936-59-4) + 3-Chloro-2-methylpropene (563-47-3) → 1-chloro-5-methyl-3-phenylhex-5-en-3-ol (1110641-65-0)

Conditions	Yield
Stage #1: 3-Chloro-2-methylpropene With diisobutylaluminium hydride; magnesium In tetrahydrofuran; hexane at 20 - 30℃; for 2h; Inert atmosphere; Stage #2: With cerium(III) chloride In tetrahydrofuran; hexane at -10℃; for 0.5h; Inert atmosphere; Stage #3: 3-chloropropiophenone	95%
Stage #1: 3-Chloro-2-methylpropene With diisobutylaluminium hydride; magnesium at 20 - 30℃; for 2h; Inert atmosphere; Stage #2: 3-chloropropiophenone With cerium(III) chloride In tetrahydrofuran; hexane at -10 - 0℃; for 1h; Stage #3: With hydrogenchloride In tetrahydrofuran; hexane; water at 30℃;	95%
Stage #1: 3-Chloro-2-methylpropene With diisobutylaluminium hydride; magnesium In tetrahydrofuran; hexane at 20 - 30℃; Inert atmosphere; Stage #2: With cerium(III) chloride In tetrahydrofuran; hexane at -10 - 20℃; Inert atmosphere; Stage #3: 3-chloropropiophenone
Stage #1: 3-Chloro-2-methylpropene With diisobutylaluminium hydride; magnesium In tetrahydrofuran; hexane at 20 - 30℃; Inert atmosphere; Stage #2: With cerium(III) chloride In tetrahydrofuran; hexane at -10 - 20℃; Inert atmosphere; Stage #3: 3-chloropropiophenone In tetrahydrofuran; hexane at -10 - 0℃;
Stage #1: 3-Chloro-2-methylpropene With diisobutylaluminium hydride; magnesium In tetrahydrofuran; hexane at 20 - 30℃; for 2h; Inert atmosphere; Stage #2: 3-chloropropiophenone With cerium(III) chloride In tetrahydrofuran; hexane at 0℃; for 0.5h; Inert atmosphere; Stage #3: With hydrogenchloride; water In tetrahydrofuran; hexane at 30℃;

Upstream product

• 71-43-2 benzene 
• 29526-96-3 1-phenylcyclopropan-1-ol 
• 93-89-0 benzoic acid ethyl ester 
• 2687-12-9 cinnamyl chloride 
• 93-55-0 1-phenyl-propan-1-one 
• 104-52-9 phenylpropyl chloride 
• 50-00-0 formaldehyd 
• 98-86-2 acetophenone 
• 18776-12-0 3-chloro-1-phenyl-propan-1-ol 
• 7647-01-0 hydrogenchloride 
• 64-19-7 acetic acid 
• 2674-04-6 diphenyl cadmium 
• 625-36-5 2-chloropropionyl chloride 
• 768-03-6 Phenyl vinyl ketone 

Downstream Products

• 855288-74-3 phenyl[1, 1’; 4’, 1’’]terphenyl-2’-yl-methanone 
• 858858-92-1 1-biphenyl-4-yl-2,5-diphenyl-pentane-1,5-dione 
• 768-03-6 Phenyl vinyl ketone 
• 18792-80-8 1-phenylbenzanthrone 
• 211059-29-9 10-(3-oxo-3-phenylpropyl)-9-(10H)-anthracenone 
• 52236-44-9 10,10-bis(3-oxo-3-phenylpropyl)-9-(10H)-anthracenone 
• 97427-62-8 4,4-bismethoxycarbonyl-1-oxo-1-phenylbutane 
• 77-35-0 3-chloro-1-cyclohexyl-1-phenyl-propan-1-ol 
• 7404-85-5 3-Methoxycarbonyl-3-cyan-1,5-dibenzoyl-pentan 
• 98013-04-8 1,3,5-tribenzoylcyclohexane 
• 97802-12-5 4-p-biphenylyl-7-phenyl-1,10-phenanthroline 
• 17109-22-7 N-methyl-N-(3-oxo-3-phenylpropyl)acetamide 
• 215392-06-6 3-[(2-Hydroxy-2-phenyl-ethyl)-methyl-amino]-1-phenyl-propan-1-one 
• 215391-90-5 3-[Benzyl-((R)-3-hydroxy-3-phenyl-propyl)-amino]-1-phenyl-propan-1-one 

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