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16096-32-5

Basic Information
CAS No.: 16096-32-5
Name: 4-Methylindole
Article Data: 46
Molecular Structure:
Molecular Structure of 16096-32-5 (4-Methylindole)
Formula: C9H9N
Molecular Weight: 131.177
Synonyms: 4-Methyl-1H-indole;
EINECS: 240-262-5
Density: 1.11 g/cm3
Melting Point: 5 °C
Boiling Point: 267.821 °C at 760 mmHg
Flash Point: 114.058 °C
Solubility: insoluble in water
Appearance: clear yellow to brown liquid after melting
Hazard Symbols: IrritantXi
Risk Codes: 36/37/38
Safety: 24/25-36-26 37/39
PSA: 15.79000
LogP: 2.47630
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    Product Name: 4-Methylindole CAS: 16096-32-5 MF: C9H9N MW: 131.17 EINECS: 240-262-5 Mol File: 16096-32-5.mol 4-Methylindole Structure 4-Methylindole Chemical Properties Melting point 5 °C Boiling point 267 °C dens

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    4-Methylindole

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    4-Methylindole

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Specification

The 4-Methylindole, with the CAS registry number 16096-32-5, is also known as Indole, 4-methyl-. It belongs to the product categories of Blocks; Indoles Oxindoles; Indoles and Derivatives; Pyrroles & Indoles; Indoles; Simple Indoles; Pyrroles & Indoles. Its EINECS registry number is 240-262-5. This chemical's molecular formula is C9H9N and molecular weight is 131.17. What's more, both its IUPAC name and systematic name are the same which is called 4-Methyl-1H-indole.

Physical properties about 4-Methylindole are: (1)ACD/LogP: 2.54; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.54 ; (4)ACD/LogD (pH 7.4): 2.54; (5)ACD/BCF (pH 5.5): 50.17; (6)ACD/BCF (pH 7.4): 50.17; (7)ACD/KOC (pH 5.5): 573.80; (8)ACD/KOC (pH 7.4): 573.80; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 15.79 Å2; (13)Index of Refraction: 1.655; (14)Molar Refractivity: 43.353 cm3; (15)Molar Volume: 118.147 cm3; (16)Polarizability: 17.187×10-24cm3; (17)Surface Tension: 46.40 dyne/cm; (18)Density: 1.11 g/cm3; (19)Flash Point: 114.058 °C; (20)Enthalpy of Vaporization: 48.548 kJ/mol; (21)Boiling Point: 267.821 °C at 760 mmHg ; (22)Vapour Pressure: 0.013 mmHg at 25 °C.

Uses of 4-Methylindole: (1) it is used as organic synthetic reagent; (2) it is used to produce other chemicals. For example, it can react with acetic acid to get N-ethyl-4-methylindoline. This reaction needs reagent NaBH3CN at temperature of 50 °C. The reaction time is 4 hours. The yield is 60 %.

4-Methylindole  can react with acetic acid to get N-ethyl-4-methylindoline.

When you are dealing with this chemical, you should be very careful. This chemical is inflammation to the skin, eyes and respiratory system or other mucous membranes. Therefore, you should wear suitable protective clothing and avoid contacting with skin and eyes. In case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1) SMILES: c1(cccc2c1ccn2)C
(2) InChI: InChI=1S/C9H9N/c1-7-3-2-4-9-8(7)5-6-10-9/h2-6,10H,1H3
(3) InChIKey: PZOUSPYUWWUPPK-UHFFFAOYSA-N