1-bromo-2-pentyne

CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1603
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1605
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1607
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1670
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1673
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1675
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2175
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2178
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2180
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2216
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2219
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2221
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2274
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2277
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2279
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[Br-]
Reaction #384468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC#CCC(C)(C)C(=O)CP(=O)(OC)OC
Reaction #702391
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_02
CCC#CCOC(=O)c1ccc(OC(C)CCCC(C)C)cc1
Reaction #788503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #828782
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #828785
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
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