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219452

CCCCCCCCCC(C)(C)c1cc(Br)ccc1O
Reaction #50652
4-bromo-2-(1,1-dimethyldecyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)(C)c1cc(Br)ccc1OC
Reaction #50653
4-bromo-2-(1,1-dimethyldecyl) anisole
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(Br)cc2c1OC(C)(C)CC2(C)C
Reaction #52375
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Br)ccc1O
Reaction #54103
18
Ausbeute 181.2%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Br)cc1C(O)c1ccccc1
Reaction #54104
19
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Br)cc1Cc1ccccc1
Reaction #54105
20
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Br)cc1Cc1ccccc1
Reaction #54106
21
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(CCC#N)cc2CC(C)C)cc1Cc1cccc2ccccc12
Reaction #54118
3-(2-Isobutyl-4′-methoxy-3′-naphthalen-1-ylmethyl-biphenyl-4-yl)propionitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(CCC(=O)O)ccc1-c1ccc(-c2ccc(OCC(=O)O)c(Cc3cccc4ccccc34)c2CC(C)C)cc1
Reaction #54126
3-(4-(Carboxymethoxy)-2,2″-diisobutyl-3-naphthalen-1-ylmethyl-[1,1′:4′,1″]-terphenyl-4″-yl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #57573
(2-acetyl-4-bromo-phenoxy)-acetic acid ethyl ester
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)O)oc2ccc(Br)cc12
Reaction #57574
5-bromo-3-methyl-benzofuran-2-carboxylic acid
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #59025
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)ccc1OCC(=O)O
Reaction #59026
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCOc2ccc(Br)cc21
Reaction #60348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(c1ccccc1)c1cc(Br)ccc1OCc1ccccc1
Reaction #78867
(±)-3-(2-Benzyloxy-5-bromophenyl)-3-phenylpropionic Acid Methyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccccc1
Reaction #78868
3-phenylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(Br)cc2c1OC(C)(C)CC2(C)C
Reaction #79944
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #82227
ethyl (2-acetyl-4-bromophenyl)oxyacetate
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc([N+](=O)[O-])c(Br)cc1C(C)(C)C
Reaction #161180
methyl (2-tert-butyl-4-bromo-5-nitrophenyl) carbonate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(Br)c([N+](=O)[O-])cc1O
Reaction #161181
2-tert-butyl-4-bromo-5-nitro-phenol
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
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