Catalog No.:AA0033HQ

703-80-0 | 3-Acetylindole

Name: Name:3-Acetylindole
Brand: AABLOCKS
SKU: AA0033HQ
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0033HQ

Chemical Name:

3-Acetylindole

CAS Number:

703-80-0

Molecular Formula:

C10H9NO

Molecular Weight:

159.1846

MDL Number:

MFCD00005626

SMILES:

CC(=O)c1c[nH]c2c1cccc2

Properties

BP:

333.9°C at 760 mmHg

Form:

Solid

MP:

188-192 °C(lit.)

Refractive Index:

1.6070 (estimate)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

190

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

2.1

Upstream Synthesis Route

576-15-8

550-44-7

703-80-0

81223-73-6

[1]ChemicalandPharmaceuticalBulletin,1988,vol.36,#10,p.3770-3779

703-80-0

1421372-66-8

[1]Patent:CN106366072,2017,A,

[2]JournalofHeterocyclicChemistry,2017,vol.54,#5,p.2898-2901

703-80-0

1421373-65-0

[1]Patent:CN106366072,2017,A,

[2]JournalofHeterocyclicChemistry,2017,vol.54,#5,p.2898-2901

Downstream Synthesis Route

120-72-9

1563-90-2

703-80-0

[1]Patent:GB869775,1959,

120-72-9

108-24-7

703-80-0

17537-64-3

[1]GazzettaChimicaItaliana,1890,vol.20,p.561 ChemischeBerichte,1890,vol.23,p.1360

703-80-0

599-91-7

(1-propyl-indol-3-yl)-aceticacidamide

[1]FiziologijaNaRastenijata,1956,vol.3,p.208,212 Chem.Abstr.,1959,p.9385

703-80-0

77-78-1

19012-02-3

[1]Tetrahedron,1998,vol.54,p.13915-13928

[2]PharmacyandPharmacologyCommunications,1999,vol.5,p.95-101

[3]LettersinOrganicChemistry,2011,vol.8,p.656-662

[4]Patent:CN106366072,2017,A.Locationinpatent:Paragraph0055;0056;0057;0058;0084;0085;0086

[5]JournalofHeterocyclicChemistry,2017,vol.54,p.2898-2901

[6]JournaloftheChemicalSociety,1957,p.4810,4812

[7]JournalofHeterocyclicChemistry,2007,vol.44,p.793-801

[8]AsianJournalofChemistry,2020,vol.32,p.244-248

1477-50-5

108-24-7

703-80-0

17537-64-3

[1]GazzettaChimicaItaliana,1888,vol.18,p.406 GazzettaChimicaItaliana,1889,vol.19,p.107

[2]ChemischeBerichte,1888,vol.21,p.1930 GazzettaChimicaItaliana,1888,vol.18,p.387

Literature

Title: Synthesis of carbazolones and 3-acetylindoles via oxidative C-N bond formation through PIFA-mediated annulation of 2-aryl enaminones.

Journal: Organic & biomolecular chemistry 20120514

Title: Thionations using a P4S10-pyridine complex in solvents such as acetonitrile and dimethyl sulfone.

Journal: The Journal of organic chemistry 20110318

Title: Characterization of cytochrome P450 monooxygenase CYP154H1 from the thermophilic soil bacterium Thermobifida fusca.

Journal: Applied microbiology and biotechnology 20110301

Title: Synthesis and antiviral activity of new indole-based heterocycles.

Journal: Chemical & pharmaceutical bulletin 20101101

Title: Anti HIV-1 agents 5: synthesis and anti-HIV-1 activity of some N-arylsulfonyl-3-acetylindoles in vitro.

Journal: Bioorganic & medicinal chemistry letters 20100615

Title: Formyl- and acetylindols: vibrational spectroscopy of an expectably pharmacologically active compound family.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20091201

Title: Synthesis and evaluation of 1-(benzo[b]thiophen-2-yl)ethanone analogues as novel anti-osteoporosis agents acting on BMP-2 promotor.

Journal: Bioorganic & medicinal chemistry letters 20090801

Title: Evaluation of indole-based probes for high-throughput screening of drug binding to human serum albumin: Analysis by high-performance affinity chromatography.

Journal: Journal of separation science 20090401

Title: Low-temperature study of 3-acetylindole at 110 K.

Journal: Acta crystallographica. Section C, Crystal structure communications 20080701

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