butane

[Li][c]1cccc2c1OC(F)(F)O2
Reaction #65869
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
[Li][c]1cccc2c1OC(F)(F)O2
Reaction #65870
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC.CCC.CCCC
Reaction #164093
ethane propane n-butane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC.CCC.CCCC
Reaction #164094
ethane propane n-butane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)[Si](C)(C)OCCCCC1(C#N)CCN(C(=O)OCc2ccccc2)CC1
Reaction #175570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCC(C(=O)O)(C(=O)O)c1ccccc1
Reaction #310963
Carboxyphenylstearic acid
Yield 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
CC(C)C[N-]CC(C)C.CC(C)[N-]C(C)C.[Li+]
Reaction #362288
lithium diisopropylamide diisobutylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COc1ccc(C2(CO)CCC(OC)(OC)CC2)cc1OC1CCCC1
Reaction #383871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1OC(=O)c2ccccc21
Reaction #462209
phthalic anhydride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CCCC(C)C[O][Mg][Cl]
Reaction #501853
2-Methylpentyloxymagnesium Chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
[Cl][Mg][O]c1ccccc1
Reaction #501854
Phenoxymagnesium Chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CCCC(C)C[O][Mg][Cl]
Reaction #501855
2-methyl-1-pentyloxymagnesium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(C)=CCO
Reaction #524131
3-methyl-2-butene-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
[Li][c]1cccc2c1OC(F)(F)O2
Reaction #526808
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
[Li][c]1cccc2c1OC(F)(F)O2
Reaction #526809
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CC(CC(=O)[C@@H]1CCCN1C)=NO
Reaction #527256
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCC(C)c1ccccc1
Reaction #660703
Sec-Butylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
—
Reaction #683896
11.1
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
—
Reaction #683897
10.5
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
O=C(O)C1=CCc2ccccc21
Reaction #741629
indene-3-carboxylic acid
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
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