6-Chlorooxindole

Name: 6-Chlorooxindole | 56341-37-8
Brand: US-CATO
SKU: S57C3D-6178_10_MG
Price: 19998.0 USD
Availability: InStock

Cat. No S57C3D-6178_10_MG

Vendor: US-CATO

Product Information

Product Name

6-Chlorooxindole

Brand Name

US-CATO

Product Number

C3D-6178

CAS

56341-37-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

736344

IUPAC Name

6-chloro-1,3-dihydroindol-2-one

InChI Key

CENVPIZOTHULGJ-UHFFFAOYSA-N

SMILES

C1C2=C(C=C(C=C2)Cl)NC1=O

References

An efficient one-pot synthesis and docking studies of bioactive new antiproliferative dispiro[oxindole/acenaphthylenone‒benzofuranone] pyrrolidine scaffolds

Publication Name: Molecular Diversity

Publication Date: 2023-11-08

DOI: 10.1007/s11030-023-10741-4

Keggin-type heteropoly-11-molybdo-1-vanadophosphoric acid supported montmorillonite K-10 clay-catalysed one-pot multi-component synthesis of chromeno[2,3-b]indoles

Publication Name: Research on Chemical Intermediates

Publication Date: 2021-05-11

DOI: 10.1007/s11164-021-04483-x

Oxindole-based chalcones: synthesis and their activity against glycation of proteins

Publication Name: Medicinal Chemistry Research

Publication Date: 2019-04-22

DOI: 10.1007/s00044-019-02345-1

The Development of New Spirooxindoles Targeting the p53–MDM2 Protein-Protein Interactions for Cancer Therapy

Publication Name: Targeting Protein-Protein Interactions by Small Molecules

Publication Date: 2018

DOI: 10.1007/978-981-13-0773-7_8

N-Aryl Hydroxamic Acids by Continuous-Flow Hydrogenation

Publication Name: Synfacts

Publication Date: 2017-03-17

DOI: 10.1055/s-0036-1590128

6-Chlorooxindole

Product Information

General Information

References

An efficient one-pot synthesis and docking studies of bioactive new antiproliferative dispiro[oxindole/acenaphthylenone‒benzofuranone] pyrrolidine scaffolds

Keggin-type heteropoly-11-molybdo-1-vanadophosphoric acid supported montmorillonite K-10 clay-catalysed one-pot multi-component synthesis of chromeno[2,3-b]indoles

Oxindole-based chalcones: synthesis and their activity against glycation of proteins

The Development of New Spirooxindoles Targeting the p53–MDM2 Protein-Protein Interactions for Cancer Therapy

N-Aryl Hydroxamic Acids by Continuous-Flow Hydrogenation