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22154

CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](n2c(Cl)nc3c(Br)c(Br)ccc32)[C@H](O)[C@@H]1O
Reaction #6445
85
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2ccccc2cc1C#N
Reaction #50736
2,3-dicyano-naphthalene
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3C(=O)c4c(Br)c(Br)c(Br)c(Br)c4C3=O)ccc(C)c2n1
Reaction #54643
8-methyl-5-(3,4,5,6-tetrabromophthalimido)-quinaldine
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2c(cc1F)C1C=CC2O1
Reaction #57065
24
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c(Br)c1Br)C1(C)C=CC2O1
Reaction #57067
26
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(Oc2ccccc2)c1
Reaction #57346
1-bromo-3-phenoxy-benzene
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=C1C2C=CC1c1c(Br)cccc12
Reaction #67687
desired product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccc(Br)c(Br)c2)CC1
Reaction #68856
title compound
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(CN2CCNCC2)cc1Br
Reaction #68857
solid
Ausbeute 108.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(F)c1)N1CCN(Cc2ccc(Br)c(Br)c2)CC1
Reaction #68865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccncn1)N1CCN(Cc2ccc(Br)c(Br)c2)CC1
Reaction #68883
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N1CCN(Cc2ccc(Br)c(Br)c2)CC1)c1ccccc1
Reaction #68888
product
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2cc(-c3ccccc3-c3ccccc3)c(-c3ccccc3-c3ccccc3)cc2-c2ccccc2-c2ccccc2)cc1
Reaction #75455
1,2,4,5-tetra-p-biphenylylbenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(OCc2ccc(COc3ccc(C(=O)OCC)cc3Cl)cc2)c(Cl)c1
Reaction #81531
1,1'-[1,4-phenylene bis(methyleneoxy)]-bis-[2-chloro-4-ethoxycarbonylbenzene]
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)c(Br)cc1N
Reaction #82015
4,5-dibromo-1,2-phenylenediamine
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c(Br)cc2[nH]c1=O
Reaction #82016
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c(Br)c([N+](=O)[O-])c2[nH]c1=O
Reaction #82017
5-nitro-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Nn1c(=O)c(=O)[nH]c2c([N+](=O)[O-])c(Br)c(Br)cc21
Reaction #82019
1-amino-5-nitro-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Br)c(Br)cc2[nH]c(=O)c(=O)[nH]c12
Reaction #82033
pure title product
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1
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