Substance
ID:354336
Names and Identifiers
IUPAC Traditional name
indole-3-acetonitrile
IUPAC name
2-(1H-indol-3-yl)acetonitrile
Synonyms
3-吲哚乙腈3-(Cyanomethyl)indoleIndolylacetonitrile吲哚-3-乙腈IANNSC 523272(3-Indolyl)acetonitrile3-Indoleacetonitrile
Registration numbers
CAS Number
EC Number
MDL Number
Beilstein Number
PubChem SID
Properties
Physical Property
Flash Point
112 °C
233.6 °F
Melting Point
33-36 °C(lit.)
33-36 °C
Boiling Point
157-160 °C/0.2 mmHg(lit.)
Safety Information
European Hazard Symbols
Harmful (Xn)GHS Signal Word
Warning
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Storage Temperature
2-8°C
Safety Statements
36/37
RTECS
AM0700000
MSDS Link
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements
P280
German water hazard class
3
GHS Hazard statements
H302-H312-H332
Risk Statements
20/21/22
Product Information
Purity
≥96.0% (GC)
Grade
purum
Empirical Formula (Hill Notation)
C10H8N2
Molecule Details
Other Notes
Plant growth activator. Promotes callus growth and shoot formation in tobacco callus11
Application
Reactant for preparation of:
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Histone deacetylase inhibitors2
• Potential kinase inhibitors3
• Kv7/KCNQ potassium channel activators4
• Kinesin-Specific MKLP-2 Inhibitor5
• Pesticides6
• Potential PET cancer imaging agents7
• Agonists of the Farnesoid X Receptor (FXR) as atherosclerosis treatment8
• Butyrylcholinesterase inhibitors9
• Necroptosis inhibitors10
Plant growth activator. Promotes callus growth and shoot formation in tobacco callus11
Application
Reactant for preparation of:
• Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Histone deacetylase inhibitors2
• Potential kinase inhibitors3
• Kv7/KCNQ potassium channel activators4
• Kinesin-Specific MKLP-2 Inhibitor5
• Pesticides6
• Potential PET cancer imaging agents7
• Agonists of the Farnesoid X Receptor (FXR) as atherosclerosis treatment8
• Butyrylcholinesterase inhibitors9
• Necroptosis inhibitors10
Molecular Spectra
No Data Available
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References
No Data Available
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