ethyl orthoformate

CCOC(=O)C(=CNC1CC1)C(=O)c1cc(F)c(-n2cccc2)cc1F
Reaction #4666
crystals
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=c1c(-c2ccccc2)coc2cc(O)ccc12
Reaction #6373
7-hydroxy-isoflavone
Ausbeute 91.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=c1c(-c2ccccc2)coc2cc(O)ccc12
Reaction #6374
7-hydroxy-isoflavone
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=c1c(-c2ccccc2)coc2cc(O)ccc12
Reaction #6375
7-hydroxy-isoflavone
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(-c2coc3cc(O)ccc3c2=O)cc1OC
Reaction #6376
7-hydroxy-3',4'-dimethoxy-isoflavone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=S1(=O)N=CN(C2CC2)c2cc(Cl)c(Cl)cc21
Reaction #46114
6,7-dichloro-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccc2c(c1)S(=O)(=O)N=CN2C1CC1
Reaction #46117
4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S1(=O)N=CNc2ccc(Cl)cc21
Reaction #46122
7-chloro-4H-1,2,4-benzothiadiazine 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(=CNc1cnsn1)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #64300
Ethyl 3-(1,2,5-thiadiazole-3-ylamino)-2-(2-methyl-3,4,6-trifluorobenzoyl)acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(OCC)c1cc(Br)cs1
Reaction #69226
4-bromo-2-(diethoxymethyl)thiophene
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(OCC)c1cc(Br)cs1
Reaction #73256
4-bromo-2-(diethoxymethyl)thiophene
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc2c(cc1OC)C(=CO)C(=O)N2
Reaction #75345
5,6-dimethoxy-3-hydroxymethylene oxindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCOC1=Cc2ccc(OC)cc2CC1
Reaction #82250
3,4-dihydro-2-ethoxy-6-methoxynaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC=C(C(C)=O)C(C)=O
Reaction #90496
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1c(=O)c2conc2n(C)c1=O
Reaction #94193
captioned compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Cn1c(=O)c2conc2n(-c2ccccc2)c1=O
Reaction #94194
captioned compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC/C=C/C=C\CC/C=C\CCCCCC(OCC)OCC
Reaction #161504
(Z,Z,E)-1,1-diethoxy-7,11,13-hexadecatriene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC=C(C(=O)OCC)C(=O)c1c(F)c(F)c(F)c(F)c1CC
Reaction #180127
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)N1C=Nc2ccncc2S1(=O)=O
Reaction #182189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc2c(c1)S(=O)(=O)N=CN2C1CC1
Reaction #196276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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