Catalog No.:AA0034AG

52351-75-4 | 6-Methoxyindoline-2,3-dione

Name: Name:6-Methoxyindoline-2,3-dione
Brand: AABLOCKS
SKU: AA0034AG
Availability: InStock
Rating: 90 (10 reviews)

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250mg

98%

in stock

$9.00 $7.00

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98%

in stock

$12.00 $8.00

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98%

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$32.00 $22.00

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10g

98%

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$61.00 $43.00

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25g

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100g

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0034AG

Chemical Name:

6-Methoxyindoline-2,3-dione

CAS Number:

52351-75-4

Molecular Formula:

C9H7NO3

Molecular Weight:

177.1568

MDL Number:

MFCD00667731

SMILES:

COc1ccc2c(c1)NC(=O)C2=O

Properties

Form:

Solid

MP:

193-195°C

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

251

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.6

Upstream Synthesis Route

6966-87-6

52351-75-4

[1]SyntheticCommunications,1994,vol.24,#4,p.533-548

[2]Patent:JP2017/81888,2017,A,.Locationinpatent:Paragraph0053;0055

[3]JournaloftheChemicalSociety-PerkinTransactions1,1997,#21,p.3261-3273

[4]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1995,vol.34,#2,p.125-128

[5]Patent:WO2009/14730,2009,A1,.Locationinpatent:Page/Pagecolumn158

[6]GazzettaChimicaItaliana,1955,vol.85,p.840,841

[7]AustralianJournalofChemistry,1958,vol.11,p.225,228

[8]JournalofOrganicChemistry,1956,vol.21,p.169

[9]JournalofMedicinalChemistry,1992,vol.35,#11,p.2085-2094

302-17-0

536-90-3

52351-75-4

[1]JournalofMedicinalChemistry,2009,vol.52,#2,p.433-444

[2]EuropeanJournalofMedicinalChemistry,2011,vol.46,#1,p.275-284

[3]EuropeanJournalofMedicinalChemistry,2016,vol.124,p.809-819

[4]OrganicLetters,2018,vol.20,#16,p.4759-4763

4306-33-6

52351-75-4

[1]Patent:WO2007/56582,2007,A1,.Locationinpatent:Page/Pagecolumn71-72

536-90-3

52351-75-4

[1]JournalofMedicinalChemistry,2007,vol.50,#1,p.21-39

[2]SyntheticCommunications,1994,vol.24,#4,p.533-548

[3]JournalofMedicinalChemistry,1992,vol.35,#11,p.2085-2094

[4]GazzettaChimicaItaliana,1955,vol.85,p.840,841

[5]Patent:JP2017/81888,2017,A,

1189051-99-7

52351-75-4

[1]Tetrahedron,2009,vol.65,#36,p.7357-7363

Downstream Synthesis Route

52351-75-4

77-78-1

35162-27-7

[1]GazzettaChimicaItaliana,1955,vol.85,p.840,841

52351-75-4

4294-95-5

[1]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.3261-3273

[2]SyntheticCommunications,1994,vol.24,p.533-548

[3]AustralianJournalofChemistry,1958,vol.11,p.225,228

[4]JournalofMedicinalChemistry,2006,vol.49,p.2440-2455

1-hydroxy-6-methoxy-indoline-2,3-dione

52351-75-4

[1]HelveticaChimicaActa,1948,vol.31,p.1392,1395

79-37-8

27191-09-9

52351-75-4

108937-87-7

[1]JournalofMedicinalChemistry,2006,vol.49,p.2440-2455

52351-75-4

100-39-0

487003-20-3

[1]Chemistry-AEuropeanJournal,2006,vol.12,p.8208-8219

[2]JournaloftheAmericanChemicalSociety,2002,vol.124,p.14826-14827

[3]JournalofMedicinalChemistry,2009,vol.52,p.433-444

[4]OrganicLetters,2018,vol.20,p.4759-4763

[5]OrganicLetters,2019,vol.21,p.9742-9746

[6]AngewandteChemie-InternationalEdition,2020,vol.59,p.442-448 Angew.Chem.,2020,vol.132,p.450-456,7

Literature

Title: Design and evaluation of a novel fluorescent CB2 ligand as probe for receptor visualization in immune cells.

Journal: Bioorganic & medicinal chemistry letters 20111001

Title: Two new alkaloids from Capparis himalayensis.

Journal: Chemical & pharmaceutical bulletin 20080201

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SDS