513830
Indole-5-carboxaldehyde
98%
Synonym(s):
5-Formylindole
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5 G
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About This Item
Empirical Formula (Hill Notation):
C9H7NO
CAS Number:
Molecular Weight:
145.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$47.88
List Price$50.40Web-Only Promotion
Available to ship onApril 22, 2025Details
Request a Bulk Order
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Quality Level
assay
98%
mp
100-103 °C (lit.)
functional group
aldehyde
SMILES string
O=Cc1ccc2[nH]ccc2c1
InChI
1S/C9H7NO/c11-6-7-1-2-9-8(5-7)3-4-10-9/h1-6,10H
InChI key
ADZUEEUKBYCSEY-UHFFFAOYSA-N
Related Categories
Application
Indole-5-carboxaldehyde can be used as a reactant in the:
- Preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents[1]
- Preparation of analogs of botulinum neurotoxin serotype A protease inhibitors[2]
- Stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes[3]
- Synthesis of para-para stilbenophanes by McMurry coupling[4]
- Stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes[5]
- Structure-based drug design of aurora kinase A inhibitors[6]
- Preparation of 5-indolyl linked 15- and 18-membered azacrown ethers to study their cation-π interactions.[7]
- Preparation of bibenzimidazole derivatives substituted 5-indolyl moiety in the study of inhibition of topoisomerase I activity.[8]
- Synthesis of (5-(4-(3,4,5-trimethoxybenzoyl)-1H-imidazol-2-yl)-1H-indol-2-yl)(3,4,5-trimethoxyphenyl)methanone[9] and radioiodinated indolochalcone.[10]
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A series of 2'-heterocyclic derivatives of 5-phenyl-2,5'-1H-bibenzimidazoles were evaluated for topoisomerase I poisoning activity and cytotoxicity. Topo I poisoning activity was associated with 2'-derivatives that possessed a hydrogen atom capable of hydrogen bond formation, suggesting that the interatomic distances between
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The synthesis of a new family of methoxy-substituted [2.7]- and [2.8]paracyclophanes linked by 3-oxapentamethylene-1,5-dioxy and hexamethylene-1,6-dioxy bridges has been carried out by using the McMurry methodology. Related indole compounds were also synthesised. Olefin-to-diol ratios depended on the bridge length, the
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Botulinum neurotoxin (BoNT), the etiological agent that causes the neuroparalytic disease botulism, has become a highly studied drug target in light of the potential abuse of this toxin as a weapon of bioterrorism. In particular, small molecule inhibitors of the
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