Production Method 1

244029-95-6

389056-99-9

6330-51-4

2376485-44-6

1003-31-2

86-84-0

5813-89-8

313516-36-8

Reaction Conditions

1.1 Solvents: Acetonitrile ;  60 min, rt

Reference

Production of Amidinyl Radicals via UV-Vis-Light Promoted Reduction of N-Arylthiophene-2-carboxamidoximes and Application to the Preparation of Some New N-Arylthiophene-2-carboxamidines

Mekhemer, Islam M. A. ; et al, ACS Omega, 2020, 5(44), 28712-28721

1H-Naphth[1,2-d]imidazole, 2-(2-thienyl)- Raw materials

• 2-Thiophenecarboximidamide, N-hydroxy-N'-1-naphthalenyl-

1H-Naphth[1,2-d]imidazole, 2-(2-thienyl)- Preparation Products

• N-Naphthalen-1-yl-formamide (6330-51-4)
• N-1-Naphthalenyl-2-thiophenecarboximidamide (2376485-44-6)
• 1H-Naphth[1,2-d]imidazole, 2-(2-thienyl)- (389056-99-9)
• Thiophene-2-carbonitrile (1003-31-2)
• 1-Naphthyl isocyanate (86-84-0)
• 2-Thiophenecarboxamide (5813-89-8)
• N-(1-naphthyl)thiophene-2-carboxamide (313516-36-8)

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