Участвует в 21 реакциях

5251

c1cncc(N2CCNCC2)c1
Reaction #216
Выход 0.0%750 AstraZeneca ELN dataset
COc1cccc(OC2CCN(c3ccc4nnc(C(F)(F)F)n4c3)CC2)c1
Reaction #227
Выход 30.5%750 AstraZeneca ELN dataset
Cn1nccc1CCOc1ccc(C2CCN(c3ccc4nnc(C(F)(F)F)n4c3)CC2)cc1
Reaction #228
Выход 19.1%750 AstraZeneca ELN dataset
CCCCCCCCCCCC
Reaction #863
dodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9850
terephthalic acid
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9851
terephthalic acid
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9852
terephthalic acid
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1nn2c(-c3ccccc3)nnc2cc1C1CCC1
Reaction #11322
title compound
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47126
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47127
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47128
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc(C(=O)O)cc1
Reaction #47132
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCO[Si](CCCCl)(OCC)OCC
Reaction #80960
3-chloropropyltriethoxysilane
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCO[Si](CCCCl)(OCC)OCC
Reaction #80961
3-chloropropyltriethoxysilane
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCO[Si](CCC(F)(F)F)(OCC)C1CCCC1
Reaction #80962
3,3,3-trifluoropropylcyclopentyldiethoxysilane
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCO[Si](CCCN=C=O)(OCC)OCC
Reaction #80963
3-isocyanatopropyltriethoxysilane
Выход 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)C(O)(C(=O)OCC)c1cc(C)ccc1C
Reaction #83842
diethyl (2,5-dimethylphenyl)-hydroxymalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COCOc1cc(C=Cc2ccc(OC(C)=O)cc2)cc(OCOC)c1
Reaction #166050
product
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Oc1cc(C=Cc2ccc(OC(=O)CCl)cc2)cc(OC(C)=O)c1
Reaction #166055
product
Выход 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Oc1ccc(C=Cc2cc(OC(C)=O)cc(OC(C)=O)c2)cc1
Reaction #166058
resveratrol triacetate
Выход 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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