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5-Methoxy-3-indolylacetonitrile_Molecular_structure_CAS_2436-17-1)
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5-Methoxy-3-indolylacetonitrile

Catalog No. 567655 Name Sigma Aldrich
CAS Number 2436-17-1 Website http://www.sigmaaldrich.com
M. F. C11H10N2O Telephone 1-800-521-8956
M. W. 186.2099 Fax
Purity 95% Email
Storage Chembase ID: 16373

SYNONYMS

Title
5-甲氧基吲哚-3-乙腈
IUPAC name
2-(5-methoxy-1H-indol-3-yl)acetonitrile
IUPAC Traditional name
2-(5-methoxy-1H-indol-3-yl)acetonitrile
Synonyms
3-(Cyanomethyl)-5-methoxyindole

DATABASE IDS

MDL Number MFCD02094163
PubChem SID 24880382
CAS Number 2436-17-1

PROPERTIES

Empirical Formula (Hill Notation) C11H10N2O
Purity 95%
Melting Point 65-69 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application
Reactant for preparation of (-)- and (+)-debromoflustramine B and its analogues as selective butyrylcholinesterase inhibitors1Reactant for preparation of carboline analogs as potent MAPKAP-K2 inhibitors2Reactant for preparation of indole-N-acetic acid derivatives as aldose reductase inhibitors for diabetic complications treatment3Reactant for preparation of debromoflustramine B and labeled Me(3a)-13C-physostigmine4Reactant for preparation of physostigmine and physovenine5Reactant for preparation of phenethyl substituted indole derivatives as melatoninergic agonists and antagonists6
Description (简体中文)
包装
5 g in glass bottle
Application
Reactant for preparation of (-)- and (+)-debromoflustramine B and its analogues as selective butyrylcholinesterase inhibitors1Reactant for preparation of carboline analogs as potent MAPKAP-K2 inhibitors2Reactant for preparation of indole-N-acetic acid derivatives as aldose reductase inhibitors for diabetic complications treatment3Reactant for preparation of debromoflustramine B and labeled Me(3a)-13C-physostigmine4Reactant for preparation of physostigmine and physovenine5Reactant for preparation of phenethyl substituted indole derivatives as melatoninergic agonists and antagonists6

REFERENCES