NMR Compound Spectrum Catalog

Experimental ¹H / ¹³C pages for common laboratory compounds. Filter by letter or carbon count, then open a compound for peak tables and stick spectra. Also try ¹H prediction and ¹³C prediction.

Browse All 2593

A–ZA 93 B 92 C 104 D 199 E 103 F 17 G 32 H 53 I 83 J 1 K 3 L 15 M 143 N 101 O 39 P 149 Q 4 R 5 S 37 T 133 U 41 V 30WX 2YZ 1 # 1113

CarbonsC1–C4 539 C5–C8 1285 C9–C12 768 C13–C18 1C19+

Showing 481–560 of 768 · formula C9–C12 · page 7/10

Name	CAS	Formula	Slug
Ethyl 3-bromobenzoate	24398-88-7	C9H9BrO2	`ethyl-3-bromobenzoate`
Ethyl 3-oxoheptanoate	7737-62-4	C9H16O3	`ethyl-3-oxoheptanoate`
Ethyl 4-hydroxyphenylacetate	17138-28-2	C10H12O3	`ethyl-4-hydroxyphenylacetate`
Ethyl 4-iodobenzoate	51934-41-9	C9H9IO2	`ethyl-4-iodobenzoate`
Ethyl 4'-chlorooxanilate	5397-14-8	C10H10ClNO3	`ethyl-4-chlorooxanilate`
Ethyl 7-bromoheptanoate	29823-18-5	C9H17BrO2	`ethyl-7-bromoheptanoate`
Ethyl cyclohexylacetate	5452-75-5	C10H18O2	`ethyl-cyclohexylacetate`
Ethyl Heptanoate	106-30-9	C9H18O2	`ethyl-heptanoate`
Ethyl Mandelate	774-40-3	C10H12O3	`ethyl-mandelate`
Ethyl oxanilate	1457-85-8	C10H11NO3	`ethyl-oxanilate`
Ethyl Phenylacetate	101-97-3	C10H12O2	`ethyl-phenylacetate`
Ethyl phenylcarbamate	101-99-5	C9H11NO2	`ethyl-phenylcarbamate`
Ethyl pivaloylacetate	17094-34-7	C9H16O3	`ethyl-pivaloylacetate`
Eucalyptol	470-82-6	C10H18O	`eucalyptol`
eugenol	97-53-0	C10H12O2	`eugenol`
Fenchol	1632-73-1	C10H18O	`fenchol`
fenthion	55-38-9	C10H15O3PS2	`fenthion`
flopropione	2295-58-1	C9H10O4	`flopropione`
Folpet	133-07-3	C9H4Cl3NO2S	`folpet`
Fosthiazate	98886-44-3	C9H18NO3PS2	`fosthiazate`
Furil	492-94-4	C10H6O4	`furil`
Furoin	552-86-3	C10H8O4	`furoin`
Gamma-nonalactone	104-61-0	C9H16O2	`gamma-nonalactone`
gamma-Phenyl-gamma-butyrolactone	1008-76-0	C10H10O2	`gamma-phenyl-gamma-butyrolactone`
Gamma-Terpinene	99-85-4	C10H16	`gamma-terpinene`
Gamma-undecalactone	104-67-6	C11H20O2	`gamma-undecalactone`
Glycidyl phenyl ether	122-60-1	C9H10O2	`glycidyl-phenyl-ether`
guaifenesin	93-14-1	C10H14O4	`guaifenesin`
Halomon	142439-86-9	C10H15Br2Cl3	`halomon`
hazelnut pyrazine	18138-04-0	C9H14N2	`hazelnut-pyrazine`
Hemimellitene	526-73-8	C9H12	`hemimellitene`
Hexyl acetoacetate	13562-84-0	C10H18O3	`hexyl-acetoacetate`
Hexyltrimethoxysilane	3069-19-0	C9H22O3Si	`hexyltrimethoxysilane`
hinokitiol	499-44-5	C10H12O2	`hinokitiol`
Hippuric acid	495-69-2	C9H9NO3	`hippuric-acid`
Homovanillic acid	306-08-1	C9H10O4	`homovanillic-acid`
Homovanillyl alcohol	2380-78-1	C9H12O3	`homovanillyl-alcohol`
Homoveratric acid	93-40-3	C10H12O4	`homoveratric-acid`
Homoveratronitrile	93-17-4	C10H11NO2	`homoveratronitrile`
Homoveratrylamine	120-20-7	C10H15NO2	`homoveratrylamine`
hydrocinnamic acid	501-52-0	C9H10O2	`hydrocinnamic-acid`
Hydroquinone bis(2-hydroxyethyl) ether	104-38-1	C10H14O4	`hydroquinone-bis2-hydroxyethyl-ether`
Hydroxyhydroquinone trimethyl ether	135-77-3	C9H12O3	`hydroxyhydroquinone-trimethyl-ether`
Indene	95-13-6	C9H8	`indene`
Indole-2-carboxylic acid	1477-50-5	C9H7NO2	`indole-2-carboxylic-acid`
indole-3-acetamide	879-37-8	C10H10N2O	`indole-3-acetamide`
indole-3-acetic acid	87-51-4	C10H9NO2	`indole-3-acetic-acid`
Indole-3-Carboxaldehyde	487-89-8	C9H7NO	`indole-3-carboxaldehyde`
Indole-3-lactic acid	1821-52-9	C11H11NO3	`indole-3-lactic-acid`
Indole-5-carboxaldehyde	1196-69-6	C9H7NO	`indole-5-carboxaldehyde`
inosine	58-63-9	C10H12N4O5	`inosine`
iodoquinol	83-73-8	C9H5I2NO	`iodoquinol`
IPTG (dioxane free)	936550-10-6	C9H18O5S	`iptg-dioxane-free`
Isoamyl butyrate	106-27-4	C9H18O2	`isoamyl-butyrate`
Isoamyl isobutyrate	2050-01-3	C9H18O2	`isoamyl-isobutyrate`
Isoamyl Isovalerate	659-70-1	C10H20O2	`isoamyl-isovalerate`
Isobutyl 2-methylvalerate	6297-42-3	C10H20O2	`isobutyl-2-methylvalerate`
Isonicoteine	581-50-0	C10H8N2	`isonicoteine`
Isononylaldehyde	5435-64-3	C9H18O	`isononylaldehyde`
Isophorone	78-59-1	C9H14O	`isophorone`
Isophorone Diamine	2855-13-2	C10H22N2	`isophorone-diamine`
Isopropyl cyclohexanecarboxylate	6553-80-6	C10H18O2	`isopropyl-cyclohexanecarboxylate`
Isopropylcyclohexane	696-29-7	C9H18	`isopropylcyclohexane`
Isoquinoline-1-carboxylic acid	486-73-7	C10H7NO2	`isoquinoline-1-carboxylic-acid`
Isoquinoline-3-carboxylic Acid	6624-49-3	C10H7NO2	`isoquinoline-3-carboxylic-acid`
Isothiochroman	4426-75-9	C9H10S	`isothiochroman`
Isovaleric anhydride	1468-39-9	C10H18O3	`isovaleric-anhydride`
Jeffcat Zf 10	83016-70-0	C9H22N2O2	`jeffcat-zf-10`
Kusol	635-46-1	C9H11N	`kusol`
kynurenic acid	492-27-3	C10H7NO3	`kynurenic-acid`
Kyowanoic n	3302-10-1	C9H18O2	`kyowanoic-n`
l-Menthol	2216-51-5	C10H20O	`l-menthol`
Lastar A	2403-88-5	C9H19NO	`lastar-a`
Lawsone	83-72-7	C10H6O3	`lawsone`
Lepidine	491-35-0	C10H9N	`lepidine`
Limonene oxide	1195-92-2	C10H16O	`limonene-oxide`
Linalool	78-70-6	C10H18O	`linalool-2`
Linuron	330-55-2	C9H10Cl2N2O2	`linuron`
m-Bis(2-hydroxyethoxy)benzene	102-40-9	C10H14O4	`m-bis2-hydroxyethoxybenzene`
m-Bromopropiophenone	19829-31-3	C9H9BrO	`m-bromopropiophenone`

References & data sources

NMRShiftDB2 — open experimental NMR chemical shift database.
Steinbeck, C.; Kuhn, S. NMRShiftDB — nmrshiftdb.nmr.uni-koeln.de
Gottlieb, H. E.; Kotlyar, V.; Nudelman, A. NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities. J. Org. Chem. 1997, 62, 7512–7515.
Fulmer, G. R. et al. NMR Chemical Shifts of Trace Impurities. Organometallics 2010, 29, 2176–2179.
PubChem — compound identifiers and structure depictions (NIH/NCBI).
Related tools: nmrdb.org (community NMR prediction reference).