sodium acetate

CON=Cc1[nH]ccc1S(=O)(=O)NC(C)(C)C
Reaction #917
title compound
Выход 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1nccc2ccccc12
Reaction #1026
1-acetyl-isoquinoline oxime
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1cc2ccccc2cn1
Reaction #1028
3-acetyl-isoquinoline oxime
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1nccc(-c2ccccn2)n1
Reaction #1029
2-acetyl-4-(pyrid-2-yl)-pyrimidine oxime
Выход 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Выход 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
Reaction #1540
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #1588
expected product
Выход 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #1656
expected product
Выход 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
ON=C1CCCc2ccccc21
Reaction #1828
product
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CN(CCO)CC(=O)O
Reaction #1932
HEIDA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCN
Reaction #2024
ethylenediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1cnc2c1c(=O)[nH]c(=O)n2C
Reaction #2083
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2161
expected product
Выход 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2202
expected product
Выход 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC(CO)CC(=O)OC
Reaction #2340
methyl 4-hydroxy-3-vinylbutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[C@@H]1C(=O)CC[C@@H]1CC(=O)OC
Reaction #2469
methyl (+)-(1R)-cis-3-oxo-2-pentyl-1-cyclopentaneacetate
Выход 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCc1cc(C=C2SC(=S)NC2=O)cc(CC=C)c1O
Reaction #3045
5-[(3,5-di-2-propenyl-4-hydroxyphenyl)-methylene]-2-thioxo-4-thiazolidinone
Выход 94.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(CC2CO2)cc(C)c1OCC1CO1
Reaction #4242
4-(2,3-epoxypropyl)-2,6-dimethylphenyl glycidyl ether
Выход 863.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Clc1cc(CC2CO2)cc(Cl)c1OCC1CO1
Reaction #4244
pale yellow resin
Выход 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
c1ccc(-c2cc(CC3CO3)cc(-c3ccccc3)c2OCC2CO2)cc1
Reaction #4245
yellow resin
Выход 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
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