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5-Chloroindole-3-carboxaldehyde, 98%|404592|827-01-0

5-Chloroindole-3-carboxaldehyde, 98%

Cat. No JK404592_1_G
J&K Chemical

Product Information

Product Name
5-Chloroindole-3-carboxaldehyde, 98%
Brand Name
J&K
Product Number
404592
CAS
827-01-0
Molecular Formula
C9H6ClNO
Molecular Weight
179.61
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2795374
IUPAC Name
5-chloro-1H-indole-3-carbaldehyde
InChI Key
YXEXOIGXNYITQH-UHFFFAOYSA-N
SMILES
C1=CC2=C(C=C1Cl)C(=CN2)C=O

Properties

Melting Point
213-216

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Metabolic engineering approaches for the biosynthesis of antibiotics
Publication Name: Microbial Cell Factories
Publication Date: 2025-01-31
DOI: 10.1186/s12934-024-02628-2

Thiazolo[5,4-b]indole derivatives as additives to cardioplegic solutions with increased time of preventing hypothermic ischemia
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2024-02
DOI: 10.1007/s10593-024-03297-0

Manipulation and epigenetic control of silent biosynthetic pathways in actinobacteria
Publication Name: World Journal of Microbiology and Biotechnology
Publication Date: 2024-01-09
DOI: 10.1007/s11274-023-03861-4

Visible-Light-Promoted Indole C-3 Formylation Using Eosin Y as a Photoredox Catalyst
Publication Name: Synlett
Publication Date: 2022-03-25
DOI: 10.1055/a-1777-2556

Application of CRISPR/Cas9 Editing for Production of Secondary Metabolites in Actinomycetes
Publication Name: Natural Products from Actinomycetes
Publication Date: 2022
DOI: 10.1007/978-981-16-6132-7_12

5-Chloroindole-3-carboxaldehyde, 98%

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