Teilstruktursuche

Br

CCOC(=O)Cc1ccc(Br)cc1
Reaction #1303
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(Br)c1
Reaction #1304
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(Br)cc1
Reaction #1458
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(Br)c1
Reaction #1459
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2c(Br)c(Cl)sc2c1=O
Reaction #4369
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2c(Br)c(Cl)sc12
Reaction #4375
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)N1CC(c2ccccc2)CCC1=O
Reaction #7495
ester
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(Br)=N/Nc1ccccc1Cl
Reaction #7501
title compound
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
BrCc1csc2ccccc12
Reaction #8198
3-Bromomethylbenzo[b]thiophene
Ausbeute 42.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CBr)Cc1ccccc1)NN=C(Cc1ccnc2ccccc12)c1ccccn1
Reaction #8316
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(Cc2ccccc2)CN1N=C(Cc1ccnc2ccccc12)c1ccccn1
Reaction #8324
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2c(Br)cccc21
Reaction #9377
4-Bromoindan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCNc1cc(Cl)cnc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11814
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Cc2ccc(Br)cc2)n3C)ccn1
Reaction #41767
(4-{2-[(4-bromophenyl)methyl]-1-methylbenzimidazol-5-yloxy)-(2-pyridyl))-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cccc(-n2cccn2)c1
Reaction #44062
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\C)Oc1cccc(Br)c1
Reaction #47533
(E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1cccc(Br)c1
Reaction #47534
(E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester
Ausbeute 31.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #48533
resultant solution
DOI: 10.6084/m9.figshare.5104873.v1
CCC[n+]1cn(N)cn1.[Br-]
Reaction #48534
1-n-propyl-4-amino-1,2,4-triazolium bromide
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[n+]1cn(N)cn1.[Br-]
Reaction #48535
1-ethyl-4-amino-1,2,4-triazolium bromide
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter