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CCC(=O)CBr

CCCCC1CCC(Br)C(=O)C1
Reaction #40299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC(=O)C1Br
Reaction #40333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)C(Br)c1ccccc1
Reaction #54242
1-bromo-1-phenyl-3,3-dimethyl-butan-2-one
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)c1ccccc1
Reaction #54243
1-phenyl-1-(4'-chlorophenoxy)-3,3-dimethyl-butan-2-one
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(Cn1ccnc1)(OC)c1ccc2ccccc2c1
Reaction #54820
1-[2-(2-naphthyl)-2,2-dimethoxyethyl]imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=C(C(=O)OCC(Cl)(Cl)Cl)N2C(=O)C(NC(=O)CC(=O)CBr)[C@H]2S1
Reaction #56556
2,2,2-trichloroethyl 2-methyl-7-(3 -oxo-4-bromobutyramido)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Br.CCOC(=O)C(=NOC)c1csc(N)n1
Reaction #56563
ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc[n+]1CC(=O)C1=CCCC1.[Br-]
Reaction #66100
1-(2-Cyclopent-1-enyl-2-oxo-ethyl)-2-methyl-pyridinium bromide salt
Ausbeute 117.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2csc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](OC)C3)n2)CC1
Reaction #71799
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C(Br)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
Reaction #78037
4-Bromo-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nocc1O
Reaction #80407
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)Cc1ccccc1Oc1ccc(Cl)cc1
Reaction #80587
1-bromo-3-[(4-chlorophenoxy)phenyl]-2-propanone
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CC(O)(COc3ccc(Cl)cc3)N=C2c2ccc(Cl)cc2)cc1
Reaction #80588
2-(4-chlorophenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-[(4-chlorophenoxy)methyl]-4,5-dihydro-1H-imidazole
Ausbeute 35.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)CC(=O)Nc1ccc(N2CCOCC2)c(F)c1
Reaction #84533
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1cccc(F)c1)CC(=O)Nc1ccc(N2CCOCC2)c(F)c1
Reaction #84534
title compound
Ausbeute 2.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N=c2ccc(I)cn2C(C)C(=O)C2CC2)cc1
Reaction #88659
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)C(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)COP(=O)(O)O
Reaction #164456
Bromoacetyl Glucose-6-Phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(C)(C)C(Br)C1=O
Reaction #165683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(C)(C)c2sc(N)nc21
Reaction #165684
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)C(=O)CN=[N+]=[N-])ccc1F
Reaction #171044
1-azido-3-(4-fluoro-3-methoxyphenyl)-3-methylbutan-2-one
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
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