Catalog No.:AA006WRA

4837-74-5 | 2-(4-Methoxy-1H-indol-3-yl)acetonitrile

Name: Name:2-(4-Methoxy-1H-indol-3-yl)acetonitrile
Brand: AABLOCKS
SKU: AA006WRA
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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA006WRA

Chemical Name:

2-(4-Methoxy-1H-indol-3-yl)acetonitrile

CAS Number:

4837-74-5

Molecular Formula:

C11H10N2O

Molecular Weight:

186.2099

MDL Number:

MFCD09751226

SMILES:

N#CCc1c[nH]c2c1c(OC)ccc2

Properties

BP:

408.3°C at 760 mmHg

Form:

Solid

MP:

136-138°C

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

245

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.7

Downstream Synthesis Route

90734-97-7

143-33-9

4837-74-5

N-(4-methoxyindol-3-yl)methylformamide

[1]Yamada,Fumio;Hashizume,Tomoko;Somei,Masanori[Heterocycles,1998,vol.47,#1,p.509-516]

90734-97-7

4837-74-5

[1]Yamada,Fumio;Kobayashi,Kensuke;Shimizu,Aya;Aoki,Naokatsu;Somei,Masanori[Heterocycles,1993,vol.36,#12,p.2783-2804]

[2]Yamada,Fumio;Kobayashi,Kensuke;Shimizu,Aya;Aoki,Naokatsu;Somei,Masanori[Heterocycles,1993,vol.36,#12,p.2783-2804]

[3]Pedras,M.SoledadeC.;Yaya,EstifanosE.[OrganicandBiomolecularChemistry,2013,vol.11,#7,p.1149-1166]

Literature

Title: Anti-inflammatory effects of 7-hydroxyl-1-methylindole-3-acetonitrile, a synthetic arvelexin derivative, on the macrophages through destabilizing mPGES-1 mRNA and suppressing NF-κB activation.

Journal: Chemico-biological interactions 20141205

Title: Alkaloids from the root of Isatis indigotica.

Journal: Journal of natural products 20120622

Title: 2-(4-Meth-oxy-1H-indol-3-yl)acetonitrile.

Journal: Acta crystallographica. Section E, Structure reports online 20120101

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SDS