Recherche de Sous-structure

ClCBr

O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1033
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1036
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CC(O)C(Cl)(Br)C(F)(F)F
Reaction #1339
5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CC(O)C(Cl)(Br)C(F)(F)F
Reaction #1340
5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene
Rendement 73.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(OC)OC(C=C(C)C)C(Cl)(Br)C(F)(F)F
Reaction #1341
5-bromo-5-chloro-4-(1,1-dimethoxyethoxy)-2-methyl-6,6,6-trifluorohex-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)(C)C=CC(Cl)(Br)C(F)(F)F
Reaction #1342
methyl 6-bromo-6-chloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CC(O)C(Cl)(Br)C(F)(F)F
Reaction #3108
5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CC(O)C(Cl)(Br)C(F)(F)F
Reaction #3109
5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene
Rendement 73.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(OC)OC(C=C(C)C)C(Cl)(Br)C(F)(F)F
Reaction #3110
5-bromo-5-chloro-4-(1,1-dimethoxyethoxy)-2-methyl-6,6,6-trifluorohex-2-ene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)(C)C=CC(Cl)(Br)C(F)(F)F
Reaction #3111
methyl 6-bromo-6-chloro-3,3-dimethyl-7,7,7-trifluorohept-4-enoate
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)O)C1C(C(Cl)(Br)C(F)(F)F)S(C)(=O)=O
Reaction #5737
2,2-dimethyl-3-[2-trifluoromethyl-2-bromo-2-chloro-1-methylsulfonylethyl]-cyclopropane carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2cccc(Br)n2n1
Reaction #9277
title compound
Rendement 73.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2cccc(Br)n2n1
Reaction #9289
title compound
Rendement 64.8%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn2c(Br)cccc2c1NC(=O)OC(C)(C)C
Reaction #9302
tert-butyl N-[7-bromo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCl)c1=O
Reaction #40951
title compound
Rendement 98.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2cn(CCCCCl)c(=O)[nH]c2=O)n1
Reaction #40960
title compound
Rendement 157.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2c(Br)cccc2C1O
Reaction #49510
3-hydroxy-7-bromo-2-(1-methyl-1-phenylethyl)isoindolinone
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Br
Reaction #50106
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Br)C1
Reaction #50107
epoxide
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C1=C(CC2)N(CC2CC2)CC1
Reaction #54676
oxygen
DOI: 10.6084/m9.figshare.5104873.v1
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