246239
6-Chloroindole
99%
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About This Item
Empirical Formula (Hill Notation):
C8H6ClN
CAS Number:
Molecular Weight:
151.59
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-449-4
Beilstein/REAXYS Number:
112345
MDL number:
Assay:
99%
Form:
solid
Quality Level
assay
99%
form
solid
mp
87-90 °C (lit.)
solubility
ethanol: 50 mg/mL, clear, colorless to faintly yellow
functional group
chloro
SMILES string
Clc1ccc2cc[nH]c2c1
InChI
1S/C8H6ClN/c9-7-2-1-6-3-4-10-8(6)5-7/h1-5,10H
InChI key
YTYIMDRWPTUAHP-UHFFFAOYSA-N
General description
6-Chloroindole, when added to Claviceps purpurea, produced the corresponding substituted L-tryptophan.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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D S Fukuda et al.
Applied microbiology, 21(5), 841-843 (1971-05-01)
Claviceps purpurea has been shown to produce extracellular l-tryptophan from indole in stirred fermentors. The substrate specificity of this conversion was investigated by using substituted indoles, anthranilic acid, and 4-chloro-anthranilic acid. Addition of 2-, 4-, 5-, 6-, and 7-methyl indole
Jeongchan Lee et al.
Nature chemical biology, 17(1), 104-112 (2020-11-04)
Tyrian purple, mainly composed of 6,6'-dibromoindigo (6BrIG), is an ancient dye extracted from sea snails and was recently demonstrated as a biocompatible semiconductor material. However, its synthesis remains limited due to uncharacterized biosynthetic pathways and the difficulty of regiospecific bromination.
Chaitany Jayprakash Raorane et al.
Biomolecules, 10(8) (2020-08-23)
Multi-drug resistant Acinetobacter baumannii is well-known for its rapid acclimatization in hospital environments. The ability of the bacterium to endure desiccation and starvation on dry surfaces for up to a month results in outbreaks of health care-associated infections. Previously, indole