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I3408

Indole

≥99%

Synonym(s):

1H-Benzo[b]pyrrole

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About This Item

Empirical Formula (Hill Notation):

C₈H₇N

CAS Number:

Molecular Weight:

117.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

EC Number:

204-420-7

Beilstein/REAXYS Number:

107693

MDL number:

Assay:

≥99%

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Properties

Quality Level

assay

≥99%

bp

253-254 °C (lit.)

mp

51-54 °C (lit.)

SMILES string

c1ccc2[nH]ccc2c1

InChI

1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H

InChI key

SIKJAQJRHWYJAI-UHFFFAOYSA-N

Description

Application

Indole is a nitrogen-containing heterocycle used in the total synthesis of compounds such as goniomitine, (−)-isatisine A, and (±)-aspidospermidine.
It is used as an electron donor moiety in synthesizing dyes for organic photovoltaics.
It can also be used in the preparation of indole based conjugated small molecules for nonlinear optics applications.

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pictograms

Skull and crossbones

Environment

signalword

Danger

hcodes

H302,H311,H319,H400

pcodes

P264 - P273 - P280 - P301 + P312 - P302 + P352 + P312 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_f

249.8 °F - closed cup

flash_point_c

121 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Synthesis and nonlinear optical properties of novel conjugated small molecules based on indole donor

Liu J, et al.

Journal of Molecular Structure, 1165(30), 223-227 (2018)

Synthesis of double D-A branched organic dyes employing indole and phenoxazine as donors for efficient DSSCs

Hong Y, et al.

Tetrahedron, 70(36), 6296-6302 (2014)

Total Synthesis of (−)-Isatisine A

Zhang X, et al.

Angewandte Chemie (International ed. in English), 50(27), 6164-6166 (2011)

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Global Trade Item Number

SKU	GTIN
I3408-100G	04061833856116
I3408-25G	04061833856123
I3408-500G	04061833856130