oxalic acid dihydrate

Cc1cccc(O)c1C=O
Reaction #883
m-cresol formaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cc1ccc2ccccc2n1)NC(CCN1CCCC1)c1ccccc1.O=C(O)C(=O)O
Reaction #63278
subject compound
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1ccc(C(CCN2CCCCC2)NC(=O)Cc2ccc3ccccc3n2)cc1.O=C(O)C(=O)O
Reaction #63286
subject compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1ccc(C(CCN2CCCCC2)NC(=O)Cc2ccc3ccccc3n2)cc1.O=C(O)C(=O)O
Reaction #63288
subject compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COCc1c(OC)nc(C(C)C)c(/C=C/C=O)c1-c1ccc(F)cc1
Reaction #65196
(E)-3-[4-(4-Fluorophenyl)-6-isopropyl-2-methoxy-3-methoxymethyl-pyridin-5-yl]-prop-2-enal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cccc(O)c1C=O
Reaction #65310
m-cresolformaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C=Cc1ccc(O)cc1.Oc1cccc2ccccc12
Reaction #65311
1-naphthol methylene-p-cresol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCNC(=O)[C@@H](N)CO
Reaction #81636
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Br)c(Br)cc2[nH]c1=O
Reaction #82016
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Cl)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82045
title compound
المردود 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82051
title compound
المردود 71.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(F)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82056
pure title compound
المردود 58.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Cl)c(C(F)(F)F)cc2[nH]c1=O
Reaction #82062
title compound
المردود 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(F)c(C(F)(F)F)cc2[nH]c1=O
Reaction #82069
title compound
المردود 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(F)cc([N+](=O)[O-])c2[nH]c1=O
Reaction #82081
7-fluoro-5-nitro-1,4-dihydro-2,3-quinoxalinedione
المردود 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(C(F)(F)F)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82085
5,7-bis(trifluoromethyl)-1,4-dihydro-2,3-quinoxalinedione
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Br)c(Br)cc2[nH]c1=O
Reaction #82604
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Cl)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82633
title compound
المردود 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82639
title compound
المردود 71.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c2cc(Cl)c(C(F)(F)F)cc2[nH]c1=O
Reaction #82650
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
الصفحة 1التالي