346577-67-1

Basic information

• Product Name: 1′-benzyl-5′-ethoxyspiro[cyclohexane-1,3′-indoline]-2′,4-dione
• Synonyms: 1′-benzyl-5′-ethoxyspiro[cyclohexane-1,3′-indoline]-2′,4-dione
• CAS NO: 346577-67-1
• Molecular Weight: 349.43
• Mol File: 346577-67-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1′-benzyl-5′-ethoxyspiro[cyclohexane-1,3′-indoline]-2′,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1′-benzyl-5′-ethoxyspiro[cyclohexane-1,3′-indoline]-2′,4-dione(346577-67-1)
• EPA Substance Registry System: 1′-benzyl-5′-ethoxyspiro[cyclohexane-1,3′-indoline]-2′,4-dione(346577-67-1)

Safety Data

• Hazardous Substances Data: 346577-67-1(Hazardous Substances Data)

Upstream product

• 813445-32-8 ethyl 7-oxo-1,4-dioxaspiro[4.5]decane-8-carboxylate 
• 346577-70-6 N-benzyl-2-diazo-N-(4-ethoxy-phenyl)-malonamic acid methyl ester 
• 346577-63-7 N-benzyl-N-(4-ethoxyphenyl)-2-diazo-3-oxobutanamide 
• 346577-65-9 1-benzyl-5-ethoxy-2-indolinone 
• 156-43-4 4-Ethoxyaniline 
• 100-52-7 benzaldehyde 
• 72753-31-2 N-benzyl-N-(4-ethoxyphenyl)amine 
• 15484-91-0 N-benzylidene-4-ethoxyaniline 
• 346577-66-0 1'-benzyl-5'-ethoxyspiro[cyclohexane-1,3'-indoline]-4,2'-dione cyclic 4-ethylene ketal 

Downstream Products

• 185913-78-4 1-[4-(N-tert-butyl-carbamoyl)-2-methoxybenzene sulphonyl]-5-ethoxy-3-spiro-[4-(2-morpholinoethoxy)cyclohexane]indol-2-one; equatorial isomer 
• 185913-78-4 1'-[2-methoxy-4-(tert-butylaminocarboxamido)benzenesulfonyl]-5'-ethoxy-4-[2-(4-morpholino)ethoxy]spiro[cyclohexane-1,3'-indolin]-2'-one 
• 346577-69-3 1'-benzyl-5'-ethoxy-4-[2-(4-morpholino)ethoxy]spiro[cyclohexane-1,3'-indolin]-2'-one 
• 346577-71-7 1'-benzyl-5'-ethoxy-4-[2-(4-morpholino)ethoxy]spiro[cyclohexane-1,3'-indolin]-2'-one 
• 346577-68-2 1'-benzyl-5'-ethoxy-4-hydroxyspiro[cyclohexane-1,3'-indolin]-2'-one 
• 948551-98-2 1'-benzyl-5'-ethoxy-4-hydroxyspiro[cyclohexane-1,3'-indolin]-2'-one 

Relevant articles and documents

Application of copper(II)-mediated radical cross-dehydrogenative coupling to prepare spirocyclic oxindoles and to a formal total synthesis of Satavaptan

Application of radical cross-dehydrogenative coupling (CDC) procedures to prepare a range of novel spirocyclic oxindoles and to a formal total synthesis of the vasopressin V2 receptor antagonist Satavaptan is reported. The key step involves a c