Substructure Search

O=C(O)C1CCCC1

Nc1cc([N+](=O)[O-])ccc1SCCCCl
Reaction #79238
2-[(3-chloropropyl)sulfanyl]-5-nitrophenylamine
Yield 17.0%DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc([N+](=O)[O-])ccc1SCCCCl
Reaction #79239
1-{2-[(3-chloropropyl)sulfanyl]-5-nitrophenyl}hydrazine
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(SCCCCl)c2[nH]c3c(c12)CNCC3
Reaction #79240
3-chloropropyl 9-nitro-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-6-yl sulfide
Yield 96.9%DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc([N+](=O)[O-])ccc1SCCCCl
Reaction #199668
DOI: 10.1039/C8SC04228D
Nc1cc([N+](=O)[O-])ccc1SCCCCl
Reaction #1852019
2-[(3-chloropropyl)sulfanyl]-5-nitrophenylamine
Yield 17.0%DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc([N+](=O)[O-])ccc1SCCCCl
Reaction #1852020
1-{2-[(3-chloropropyl)sulfanyl]-5-nitrophenyl}hydrazine
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1