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18011

Cc1[nH]c2ccc([N+](=O)[O-])cc2c1C(c1ccccc1)N(C)C
Reaction #9088
Dimethyl-[(2-methyl-5-nitro-1H-indol-3-yl)-phenylmethyl]-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(CO)cc2c1
Reaction #11256
(5-nitro-1H-indol-2-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2cc([N+](=O)[O-])ccc2[nH]1
Reaction #11257
5-nitro-1H-indole-2-carbaldehyde
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(C=Cc3ccccc3Cl)cc2c1
Reaction #11258
diene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2C(c3ccccc3Cl)Cc3[nH]c4ccc([N+](=O)[O-])cc4c3C12
Reaction #11259
adduct ( 917 )
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C=O)c2cc([N+](=O)[O-])ccc2n1Cc1ccccc1
Reaction #44906
1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)O)c2cc([N+](=O)[O-])ccc2n1Cc1ccccc1
Reaction #44907
1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccc(F)c(F)c2)c2cc(N)ccc2n1Cc1ccccc1
Reaction #44908
5-amino-1-benzyl-2-methyl-1H-indole-3-carboxylic acid, 3,4-difluorobenzylamide
Ausbeute 104.3%DOI: 10.6084/m9.figshare.5104873.v1
CCNCCNC(=O)c1cc2cc([N+](=O)[O-])ccc2[nH]1
Reaction #51427
crystals
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNCCNC(=O)c1cc2cc(NC(=O)c3ccc4[nH]c(C(=O)Nc5ccc6[nH]c(C(=O)NCCNCC)cc6c5)cc4c3)ccc2[nH]1
Reaction #51428
76
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCNC(=O)c1cc2cc([N+](=O)[O-])ccc2[nH]1)C(=O)OC(C)(C)C
Reaction #51429
powder
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCNCCNC(=O)c1cc2cc(NC(=O)c3ccc4[nH]c(C(=O)Nc5ccc6[nH]c(C(=O)NCCNCCC)cc6c5)cc4c3)ccc2[nH]1
Reaction #51430
1H-Indole-2,5-dicarboxylic acid bis-{[2-(2-propylamino-ethylcarbamoyl)-1H-indol-5-yl]-amide}
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(OC)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2[nH]1
Reaction #61208
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(OC)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61209
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(O)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2[nH]1
Reaction #61211
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(O)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61212
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CSCC(F)(F)F)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2[nH]1
Reaction #61213
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CSCC(F)(F)F)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCSCC(C)(O)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2[nH]1
Reaction #61217
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c2c(c3cc([N+](=O)[O-])ccc31)CCCC2
Reaction #78883
N-isopropyl-6-nitro-1,2,3,4-tetrahydrocarbazole
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
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