614-18-6

Basic information

• Product Name: Ethyl nicotinoate
• Synonyms: RARECHEM AL BI 0185;NICOTINIC ACID ETHYL ESTER;ETHYL 3-PYRIDINECARBOXYLATE;ETHYL PYRIDINE-3-CARBOXYLATE;ETHYL NICOTINATE;ethyl nicotinoate;3-PYRIDINECARBOXYLIC ACID ETHYL ESTER;3-(Ethoxycarbonyl)pyridine
• CAS NO: 614-18-6
• Molecular Formula: C₈H₉NO₂
• Molecular Weight: 151.16
• EINECS: 210-370-7
• Product Categories: CARBOXYLICESTER;Organic acids;Heterocyclic Compounds;Aromatics;Heterocycles;Nicotine Derivatives;Building Blocks;C8 to C9;Chemical Synthesis;Heterocyclic Building Blocks;Pyridines
• Mol File: 614-18-6.mol
• Article Data: 117

Chemical Properties

• Melting Point: 8-10 °C(lit.)
• Boiling Point: 223224°C
• Flash Point: 93 °C
• Appearance: light yellow/
• Density: 1.107 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0934mmHg at 25°C
• Refractive Index: n20/D 1.504(lit.)
• Storage Temp.: 2-8°C
• Solubility: 50g/l
• PKA: pK1:3.35(+1) (25°C)
• Water Solubility: miscible
• BRN: 122937
• CAS DataBase Reference: Ethyl nicotinoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl nicotinoate(614-18-6)
• EPA Substance Registry System: Ethyl nicotinoate(614-18-6)

Safety Data

• Hazard Codes: Xi
• Statements: 37/38-41-36/38-36/37/38
• Safety Statements: 26-39-37/39-36
• WGK Germany: 3
• F: 8-9-23
• TSCA: Yes
• Hazardous Substances Data: 614-18-6(Hazardous Substances Data)

Usage

Chemical Properties

clear colourless to yellow liquid

Uses

Different sources of media describe the Uses of 614-18-6 differently. You can refer to the following data:
1. Ethyl nicotinate is a nicotinic acid derivative used for skin-conditioning cosmetics.
2. Ethyl nicotinate is used for skin-conditioning cosmetics. It is principally used in medicine as a local vasodilator at a concentration of 1 to 2 % in creams, ointments and pomades. It is utilized for the treatment sprains, wrenches, muscular pains and tendonitis.

InChI:InChI=1/C8H9NO2/c1-2-11-8(10)7-4-3-5-9-6-7/h3-6H,2H2,1H3

Synthetic route

3-iodopyridine (1120-90-7) + ethanol (64-17-5) + carbon monoxide (201230-82-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium diacetate at 20 - 125℃; under 7500.75 - 22502.3 Torr; for 0.333333h; microwave irradiation;	98%
With 1,8-diazabicyclo[5.4.0]undec-7-ene at 80℃; under 760.051 Torr; for 6h;	94%
With palladium diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene at 120℃; under 9308.91 Torr;
With palladium diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene at 120℃; under 8274.59 - 10136.4 Torr;	88 %Spectr.
With palladium diacetate; potassium carbonate at 60℃; under 20521.4 Torr; for 12h; Green chemistry; chemoselective reaction;	21 %Spectr.

3-Bromopyridine (626-55-1) + ethanol (64-17-5) + carbon monoxide (201230-82-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With triethylamine at 70℃; under 760.051 Torr; for 3h; Catalytic behavior;	98%

nicotinic acid (59-67-6) + ethanol (64-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With sulfuric acid In toluene at 55℃; for 4h;	97.2%
With sulfuric acid for 10h; Reflux; Sealed tube;	83%
With sulfuric acid for 4h; Reflux;	81%

nicotinic acid (59-67-6) + ethyl iodide (75-03-6) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With cesium fluoride In acetonitrile for 2h; Heating;	92%

1-(pyridin-3-yl)pentan-1-one (1701-72-0) + ethyl trifluoroacetate, (383-63-1) → 3-pyridinecarboxylic acid ethyl ester (614-18-6) + 1,1,1-trifluoro-2-hexanone (360-34-9)

Conditions	Yield
Stage #1: ethyl trifluoroacetate, With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Inert atmosphere; Schlenk technique; Stage #2: 1-(pyridin-3-yl)pentan-1-one In tetrahydrofuran at 0℃; for 2.5h; Inert atmosphere; Schlenk technique; Reflux; Stage #3: With hydrogenchloride In tetrahydrofuran; water at 0℃; for 0.25h; Inert atmosphere; Schlenk technique;	A 92% B n/a

dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + ethanol (64-17-5) + pyridin-3-yl 2,3,4,5,6-pentafluorobenzenesulfonate → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate at 50℃; for 12h; Schlenk technique; Inert atmosphere; chemoselective reaction;	91%

dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + ethanol (64-17-5) + pyridin-3-yl trifluoromethanesulfonate (107658-27-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate at 50℃; for 12h; Schlenk technique; Inert atmosphere; chemoselective reaction;	90%

3-iodopyridine (1120-90-7) + ethanol (64-17-5) + molybdenum hexacarbonyl (13939-06-5, 199620-15-0) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With C35H20F34NO3(1-)*Pd(2+)*Cl(1-); N-ethyl-N,N-diisopropylamine In neat (no solvent) at 130℃; for 0.333333h; Microwave irradiation;	89%

1-oxy-nicotinic acid ethyl ester (14906-63-9) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With cerium(III) chloride heptahydrate; zinc In methanol at 20℃; for 2.5h;	87%

nicotinic acid (59-67-6) + Triethyl orthoacetate (78-39-7) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
microwave irradiation;	86%
In toluene at 110℃; for 24h;	81%

ethanol (64-17-5) + nicotinamide (98-92-0) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With chloro-trimethyl-silane at 40℃; for 5h;	86%
With chloro-trimethyl-silane at 20 - 40℃; for 5h; Inert atmosphere;	86%

3-Chloropyridine (626-60-8) + dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + ethanol (64-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With (S)-1-[(R)-2-(di-1-naphthylphosphino)ferrocenyl]ethyl-di-tert.-butylphosphine; potassium acetate; palladium diacetate at 80℃; for 12h; Schlenk technique; Inert atmosphere; chemoselective reaction;	86%

ethyl bromide (74-96-4) + potassium nicotinate (16518-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With tetrabutylammomium bromide for 43h; Ambient temperature;	82%

3-Bromopyridine (626-55-1) + potassium monoethyl oxalate (1906-57-6) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With palladium(II) trifluoroacetate; 1,3-bis-(diphenylphosphino)propane In 1-methyl-pyrrolidin-2-one at 150℃; for 16h; Inert atmosphere;	82%

nicotinic acid (59-67-6) + boron trifluoride diethyl etherate (109-63-7) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
at 120℃;	82%

tetraethoxy tellurium(IV) (2017-01-8) + nicotinamide (98-92-0) → pyridine-3-carbonitrile (100-54-9) + 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
In tetrachloromethane for 18h; Heating;	A 8% B 79%

nicotinamide (98-92-0) → pyridine-3-carbonitrile (100-54-9) + 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With tetraethoxy tellurium(IV) In tetrachloromethane for 18h; Heating;	A 8% B 79%

3-iodopyridine (1120-90-7) + potassium monoethyl oxalate (1906-57-6) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With palladium diacetate In 1-methyl-pyrrolidin-2-one at 20 - 140℃; for 24h; Inert atmosphere;	79%

3-Bromopyridine (626-55-1) + dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + ethanol (64-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With dmap; palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In toluene at 90℃; for 0.5h; Microwave irradiation;	78%

nicotinic acid (59-67-6) + triethylphosphine (554-70-1) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With 1,3-diazido-propane In neat (no solvent) at 20℃; for 0.333333h;	78%

ethyl 6-iodonicotinate (151917-39-4) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With 2,6-dimethylpyridine; phenylsilane; indium(III) acetate In ethanol at 20℃; for 18h;	75%
With indium In water for 10h; Heating;	64%
With indium; water for 10h; Reflux;	64%

ethyl trifluoroacetate, (383-63-1) + C12H11NOS (1327133-50-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6) + 1,1,1-trifluoro-4-(2-thiophenyl)butan-2-one (19305-01-2)

Conditions	Yield
Stage #1: ethyl trifluoroacetate, With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Inert atmosphere; Schlenk technique; Stage #2: C12H11NOS In tetrahydrofuran at 0℃; Inert atmosphere; Schlenk technique; Stage #3: With hydrogenchloride In tetrahydrofuran; water at 0℃; for 0.25h; Inert atmosphere; Schlenk technique;	A 75% B 74%

piperidine (110-89-4) + 3-Chloropyridine (626-60-8) + carbon monoxide (201230-82-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With 1,3-bis(dicyclohexylphosphino)propane bis(tetrafluoroborate) salt; sodium phenoxide; palladium diacetate In toluene at 100℃; under 760.051 Torr; for 16h;	71%

3-Chloropyridine (626-60-8) + ethanol (64-17-5) + carbon monoxide (201230-82-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With bis(benzonitrile)palladium(II) dichloride; sodium acetate; 1,4-di(diphenylphosphino)-butane at 100℃; under 750.075 Torr; for 16h;	71%

pyridin-3-yl 4-fluorobenzenesulfonate + ethanol (64-17-5) + carbon monoxide (201230-82-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With Josiphos Et2P-Fc-PtBu2 ligand; sodium acetate; palladium diacetate at 130 - 135℃; under 2068.59 Torr; for 20h;	70%

pyrrole (109-97-7) + ethyl 2-bromo-2-diazoacetate (22736-43-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With sodium dithionite; c-type cytochrome maquette, C45 In ethanol at 5℃; for 2h; pH=8.6; Sealed tube; Inert atmosphere; Enzymatic reaction;	69.4%

pyridine-3-carbonitrile (100-54-9) + ethanol (64-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With boron trifluoride diethyl etherate for 144h; Heating;	67%
With iron(III) chloride for 21h; Heating;	63.3%

3-Bromopyridine (626-55-1) + oxalic acid diethyl ester (95-92-1) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With dmap; bis-triphenylphosphine-palladium(II) chloride In ethanol at 140℃; for 0.333333h; Microwave irradiation;	66%

Propargylamine (2450-71-7) + propynoic acid ethyl ester (623-47-2) → 3-pyridinecarboxylic acid ethyl ester (614-18-6)

Conditions	Yield
With dipotassium peroxodisulfate; silver trifluoromethanesulfonate In toluene at 80℃; for 6h; Sealed tube; regioselective reaction;	63%

3-pyridinecarboxaldehyde (500-22-1) + ethanol (64-17-5) → 3-pyridinecarboxylic acid ethyl ester (614-18-6) + 1,2-di(pyridine-3-yl)ethane-1,2-dione (35779-39-6)

Conditions	Yield
With oxygen; Thiamine hydrochloride; triethylamine for 2h; Reflux;	A 30% B 58%

2-aminobutanol (96-20-8, 13054-87-0) + 3-pyridinecarboxylic acid ethyl ester (614-18-6) → N-(1-hydroxybutan-2-yl)nicotinamide (215120-51-7)

Conditions	Yield
at 50℃; for 0.5h;	100%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 3-amino-2-propanol (78-96-6, 1674-56-2) → N-(2-hydroxypropyl)-3-pyridinecarboxamide (122048-21-9)

Conditions	Yield
at 50℃; for 0.5h;	100%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + propan-1-ol-3-amine (156-87-6) → N-(3-hydroxypropyl)nicotinamide (53676-54-3)

Conditions	Yield
at 50℃; for 0.5h;	100%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 1,3,5-tris(bromomethyl)-2,4,6-triethylbenzene (181058-08-2) → C39H48N3O6(3+)*3Br(1-)

Conditions	Yield
In acetonitrile for 6h; Heating;	100%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 2-(2-Aminoethylamino)ethanol (111-41-1) → N-(5-hydroxy-3-azapentyl)nicotinamide

Conditions	Yield
at 80 - 85℃; for 6.5h;	99.5%

3-pyridinecarboxylic acid ethyl ester (614-18-6) → Ethyl nipecotate (71962-74-8)

Conditions	Yield
With hydrogen In hexane at 100℃; under 7600.51 Torr; for 24h; Temperature; Pressure; Autoclave;	99%
With sodium hydroxide; hydrogen; nickel In ethanol; water at 20 - 40℃; Electrolysis;	98%
With 1,4-dioxane; nickel at 165℃; under 110326 - 220652 Torr; Hydrogenation;

3-pyridinecarboxylic acid ethyl ester (614-18-6) + benzyl bromide (100-39-0) → N-benzyl-3-(ethoxycarbonyl)pyridinium bromide (72551-50-9)

Conditions	Yield
In isopropyl alcohol for 18h;	98%
In isopropyl alcohol at 20℃; for 18h;	90%
In nitrobenzene at 40℃; Rate constant;
In acetone Reflux;

3-pyridinecarboxylic acid ethyl ester (614-18-6) → nicotinic acid (59-67-6)

Conditions	Yield
With PPA at 155℃; for 4.5h;	98%
With alkaline H2O In dimethyl sulfoxide at 30℃; Rate constant; other solvent (EtOH); variation of water concentrations;
esterase in WBN; IL-Ht rat abdominal skin homogenate at 37℃; Enzyme kinetics;

3-pyridinecarboxylic acid ethyl ester (614-18-6) + N-(N,N-diethylaminomethyl)-2-piperidone (86931-32-0) → sodium salt of the aminal of 3-nicotinoyl-2-piperidone

Conditions	Yield
With sodium hydride In toluene for 8h; Heating;	97%

3-pyridinecarboxylic acid ethyl ester (614-18-6) → 3-pyridinecarboxaldehyde (500-22-1)

Conditions	Yield
With n-butyllithium; diisobutylaluminium hydride; tert-butyl alcohol In tetrahydrofuran; hexane at 0℃;	97%
Multi-step reaction with 2 steps 1: diethyl ether; lithium alanate 2: lead (IV)-acetate; benzene View Scheme

3-pyridinecarboxylic acid ethyl ester (614-18-6) + ethanolamine (141-43-5) → N-(2-hydroxyethyl)nicotinamide (6265-73-2)

Conditions	Yield
Stage #1: 3-pyridinecarboxylic acid ethyl ester; ethanolamine at 125℃; for 4h; Large scale; Stage #2: With acetone at 45 - 60℃; for 1h; Large scale; Stage #3: at 10 - 30℃; for 2.5h; Temperature; Large scale;	96.6%
	64.5%
	64.5%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + guanidine hydrochloride (50-01-1) → N-(pyridyl-3-carbonyl)guanidine (6531-75-5)

Conditions	Yield
With sodium ethanolate In ethanol for 12h; Heating;	95%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 1-iodo-propane (107-08-4) → 3-ethoxycarbonyl-1-propyl pyridinium iodide

Conditions	Yield
In acetonitrile at 80℃; for 36h;	95%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + Zr(N(C5H6(CH3)4))4*4MgCl2*6LiCl + boron trifluoride diethyl etherate (109-63-7) → Zr(C5NH3BF3CO2C2H5)4

Conditions	Yield
In tetrahydrofuran dry Ar-flushed Schlenk flask charged with organic compound, soln. of base added dropwise, stirred at -78 °C for 15 min;	95%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + C10H10BrN3O + Allyl chloroformate (2937-50-0) → 1-allyl 3-ethyl 4-(5-bromo-1,3-dimethyl-2-oxoindolin-3-yl)-pyridine-1,3(4H)-dicarboxylate

Conditions	Yield
Stage #1: 3-pyridinecarboxylic acid ethyl ester; Allyl chloroformate In tetrahydrofuran at -20℃; for 0.166667h; Molecular sieve; Stage #2: C10H10BrN3O With bis(η3-allyl-μ-chloropalladium(II)) In tetrahydrofuran at -20℃; for 13h; diastereoselective reaction;	95%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + methyl methacrylate (97-63-2) → ethyl 6-(1-ethoxy-2-methyl-1-oxopropan-2-yl)nicotinate

Conditions	Yield
Stage #1: 3-pyridinecarboxylic acid ethyl ester With potassium phosphate; chloro(1,5-cyclooctadiene)rhodium(I) dimer; P,P'-(1,2-ethanediyl)bis{bis[3,5-di(trifluoromethyl)phenyl]phosphane} In toluene for 0.0833333h; Inert atmosphere; Microwave irradiation; Stage #2: methyl methacrylate In toluene at 120℃; for 24h; Inert atmosphere; Microwave irradiation; Sealed tube; regioselective reaction;	94%

3-pyridinecarboxylic acid ethyl ester (614-18-6) → Nicotinic acid hydrazide (553-53-7)

Conditions	Yield
With hydrazine hydrate monohydrate In methanol at 140℃; for 1h; Microwave irradiation; Sealed tube;	93%
With hydrazine hydrate In ethanol for 1.08333h; Ambient temperature;	85%
With hydrazine hydrate In ethanol Reflux; Sealed tube;	85%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 2,2,2-trifluoroethyl(phenyl)iodonium trifluoromethanesulfonate (100422-07-9) → N-(2,2,2-Trifluoroethyl)-3-(ethoxycarbonyl)pyridinium triflate (135654-45-4)

Conditions	Yield
In dichloromethane for 0.166667h; Ambient temperature;	93%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + benzylamine (100-46-9) → N-benzylnicotinamide (2503-55-1)

Conditions	Yield
With graphene oxide In neat (no solvent) at 100℃; for 18h; Sealed tube;	92%
With silica gel In neat (no solvent) at 100℃; for 12h; Inert atmosphere; Sealed tube;	87%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + mesitylenesulfonylhydroxylamine (36016-40-7) → 2,4,6-Trimethyl-benzenesulfonate1-amino-3-ethoxycarbonyl-pyridinium; (40146-54-1)

Conditions	Yield
In dichloromethane for 0.5h; Ambient temperature;	92%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 3-(4-bromophenyl)-2-methylquinazolin-4(3H)-one (1788-95-0) → 2-[2-Oxo-2-(3-pyridyl)ethyl]-3-p-bromophenyl-4(3H)-quinazolinone (73283-34-8)

Conditions	Yield
With sodium hydride In 1,2-dimethoxyethane Heating;	92%
	2.43 g (92%)

3-pyridinecarboxylic acid ethyl ester (614-18-6) + acetic anhydride (108-24-7) → ethyl 1-acetyl-1,4,5,6-tetrahydropyridine-3-carboxylate (917112-54-0)

Conditions	Yield
With hydrogen; palladium on activated charcoal under 5171.48 Torr;	92%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + ethyl acetate (141-78-6) → 3-oxo-3-pyridin-3-yl-propionic acid ethyl ester (6283-81-4) + ethyl acetoacetate (141-97-9)

Conditions	Yield
With lithium hexamethyldisilazane In tetrahydrofuran at -40℃; for 0.333333h; Claisen condensation; Inert atmosphere;	A 92% B n/a

3-pyridinecarboxylic acid ethyl ester (614-18-6) + 6-bromo-2-methylhexan-2-yl acetate → 1-(5-acetoxy-5-methylhexyl)-3-(ethoxycarbonyl)pyridin-1-ium bromide

Conditions	Yield
In acetonitrile for 60h; Inert atmosphere; Reflux;	92%

3-pyridinecarboxylic acid ethyl ester (614-18-6) + methyl iodide (74-88-4) → 3-(ethoxycarbonyl)-1-methylpyridin-1-ium iodide (10129-58-5)

Conditions	Yield
In nitromethane for 12h; Ambient temperature;	91%
In isopropyl alcohol for 18h;	87%
In nitrobenzene at 35℃; Rate constant;

Upstream product

• 6141-85-1 2-(3-bromophenoxy)-N-[2,6-di(propan-2-yl)phenyl]acetamide 
• 61417-99-0 8-Quinolinecarbonitrile, 5,6,7,8-tetrahydro-3,8-dimethyl- 
• 6141-78-2 tris(methylamido)thiophosphorus 
• 61417-55-8 Titanium tris(dodecylbenzenesulfonate)isopropoxide 
• 61417-50-3 Bis(4-aminobenzoato-O)(isooctadecanoato-O)(propan-2-olato)titanium 
• 614-17-5 N-ETHYLBENZAMIDE 
• 61417-49-0 Titanium triisostearoylisopropoxide 
• 61417-48-9 (11E,13E)-16-ethyl-4-hydroxy-7-(2-hydroxyethyl)-15-(hydroxymethyl)-5,9,13-trimethyl-2,10-dioxooxacyclohexadeca-11,13-dien-6-yl 3,4,6-trideoxy-3-(dimethylamino)hexopyranoside 
• 61417-47-8 6-De(2-oxoethyl)-4'-deoxy-6-methylCirramycin A1 
• 61417-46-7 DEAMINO-TYR-BETA-ALA-SECRETIN 
• 61417-20-7 2,2'-Ethynylenebisadamantane 
• 61417-19-4 1,1'-Ethynylenebisadamantane 
• 61417-13-8 10-methyl-9-({4-[(methylsulfonyl)amino]phenyl}amino)acridinium 
• 61417-10-5 N-[3-Amino-4-[(acridine-9-yl)amino]phenyl]methanesulfonamide 

Downstream Products

• 81335-77-5 Imazethapyr 
• 1187932-54-2 2-AMINO-3-PYRIDINECARBOXALDEHYDE HCL 
• 76199-85-4 2-cyano-2-[2,3-dihydro-3-(tetrahydro-2,4,6-trioxo-5(2H)-pyrimidinylidene)-1H-isoindol-1-ylidene]-N-methylacetamide 
• 7032-17-9 4-(3-AMINOPROPYL)-2,4-DIHYDRO-3H-PYRAZOL-3-ONE 

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