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Table 1 The physicochemical properties of newly synthesized derivatives (S1–S18)

From: Synthesis of thiophene derivatives and their anti-microbial, antioxidant, anticorrosion and anticancer activity

Compound

M. formula

M. Wt.

m. p. (°C)

Rf valuea

% Yield

S 1

C18H17Cl2NO2S

382.30

96–97

0.53

84.71

S 2

C18H18BrNO2S

392.31

122–124

0.47

75.00

S 3

C18H18N2O4S

358.41

87–89

0.62

82.22

S 4

C19H21NO3S

343.44

95–98

0.38

72.67

S 5

C22H28N2O2S

384.53

98–100

0.39

78.86

S 6

C19H21NO4S

359.44

95–97

0.66

82.43

S 7

C20H23NO4S

373.13

97–99

0.45

83.67

S 8

C18H18BrNO2S

392.31

94–95

0.42

87.62

S 9

C18H18ClNO2S

347.86

87–88

0.41

85.63

S 10

C18H18N2O4S

358.41

94–97

0.61

79.80

S 11

C18H18N2O4S

358.41

130–131

0.58

72.58

S 12

C18H19NO2S

313.41

90–93

0.31

68.72

S 13

C20H24N2O2S

356.48

134–135

0.53

83.23

S 14

C18H19NO3S

329.41

110–111

0.68

73.65

S 15

C18H19NO3S

329.41

108–109

0.63

81.35

S 16

C18H19NO3S

329.41

93–94

0.56

69.87

S 17

C18H19NO3S

343.44

93–95

0.55

81.81

S 18

C20H23NO4S

373.13

97–99

0.62

76.69

  1. aTLC mobile phase-benzene