1416330-52-3

Basic information

• Product Name: (R)3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)indolin-2-one
• Synonyms: (R)3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)indolin-2-one
• CAS NO: 1416330-52-3
• Molecular Weight: 409.893
• Mol File: 1416330-52-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)indolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)indolin-2-one(1416330-52-3)
• EPA Substance Registry System: (R)3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)indolin-2-one(1416330-52-3)

Safety Data

• Hazardous Substances Data: 1416330-52-3(Hazardous Substances Data)

Upstream product

• 1380195-70-9 tert-butyl 3-(benzo[d][1,3]dioxol-5-ylmethyl)-2-oxoindoline-1-carboxylate 
• 14204-31-0 2-(4-chlorophenylthio)isoindoline-1,3-dione 
• 1416330-43-2 (R)-tert-butyl 3-(benzo[d][1,3]dioxol-5-ylmethyl)-3-((4-chlorophenyl)thio)-2-oxoindoline-1-carboxylate 

Relevant articles and documents

Organocatalytic, asymmetric synthesis of 3-sulfenylated N-Boc-protected oxindoles

Sulfenylated oxindoles: The first asymmetric sulfenylation of N-Boc-protected oxindoles has been developed to provide products containing a tetrasubstituted stereogenic center in high to excellent yields (86-98 %) and, in most cases, excellent enantioselectivities (up to 96 % ee; see scheme). Copyright