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473731

7-Chloroindole

97%

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About This Item

Empirical Formula (Hill Notation):
C8H6ClN
CAS Number:
53924-05-3
Molecular Weight:
151.59
NACRES:
NA.22
PubChem Substance ID:
24870926
UNSPSC Code:
12352100
EC Number:
258-865-7
MDL number:
MFCD01321301
Assay:
97%
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Quality Level

100

assay

97%

bp

90-95 °C/0.25 mmHg (lit.)

mp

55-58 °C (lit.)

functional group

chloro

SMILES string

Clc1cccc2cc[nH]c12

InChI

1S/C8H6ClN/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,10H

InChI key

WMYQAKANKREQLM-UHFFFAOYSA-N

General description

7-Chloroindole is an indole derivative. It has been synthesized from 2,3-dihydroindole.

Application

7-Chloroindole may be used in the preparation of 1-methyl-7-chloroindole and glycosylated 7-chloroindole-3-acetamide.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000223215
0000223215
MKCL8247
MKBH1548V
00813CJ

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The chemistry of indoles. XXXIX. A facile synthetic method for 7-substituted indoles.
Somei M, et al.
Chemical & Pharmaceutical Bulletin, 35(8), 3146-3154 (1987)
Xin Teng et al.
Bioorganic & medicinal chemistry letters, 15(22), 5039-5044 (2005-09-13)
Necroptosis is a regulated caspase-independent cell death mechanism that results in morphological features resembling necrosis. It can be induced in a FADD-deficient variant of human Jurkat T cells treated with TNF-alpha. 5-(1H-Indol-3-ylmethyl)-2-thiohydantoins and 5-(1H-indol-3-ylmethyl)hydantoins were found to be potent necroptosis
Synthesis of rebeccamycin and 11-dechlororebeccamycin.
Faul MM, et al.
The Journal of Organic Chemistry, 64(7), 2465-2470 (1999)
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Global Trade Item Number

SKUGTIN
473731-1G04061825754130