533076
5-Chloroindole-3-carboxaldehyde
98%
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About This Item
Formule empirique (notation de Hill):
C9H6ClNO
Numéro CAS:
Poids moléculaire :
179.60
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Produits recommandés
Pureté
98%
Pf
213-216 °C (lit.)
Groupe fonctionnel
aldehyde
chloro
Chaîne SMILES
Clc1ccc2[nH]cc(C=O)c2c1
InChI
1S/C9H6ClNO/c10-7-1-2-9-8(3-7)6(5-12)4-11-9/h1-5,11H
Clé InChI
YXEXOIGXNYITQH-UHFFFAOYSA-N
Description générale
5-Chloroindole-3-carboxaldehyde, also known as 5-chloro-1H-indole-3-carboxaldehyde, is an indole derivative.
Application
5-Chloroindole-3-carboxaldehyde (5-Chloro-1H-indole-3-carboxaldehyde) may be used in the preparation of:
It may also be used in the preparation of the following hydrazone derivatives:
- 5-chloroindole-3-carboxaldehyde isonicotinoyl hydrazine
- 2′-[(5-chloro-1H-indol-3-yl)methylene]-2-(1H-indol-3-yl)acetohydrazide
- 5-chloro-3-(2,2-dibromovinyl)-1-(2-trimethylsilylethoxymethyl)indole
It may also be used in the preparation of the following hydrazone derivatives:
- 5-chloroindole-3-carboxaldehyde 3-chlorobenzoylhydrazone
- 5-chloroindole-3-carboxaldehyde 4-nitrobenzoylhydrazone
- 5-chloroindole-3-carboxaldehyde 3-methylbenzoylhydrazone
- 5-chloroindole-3-carboxaldehyde 4-methylbenzoylhydrazone
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Electrochemical behavior of indole-3-carboxaldehyde izonicotinoyl hydrazones: discussion on possible biological behavior
Shirinzadeh H, et al.
Combinatorial Chemistry & High Throughput Screening, 13(7), 619-627 (2010)
Tandem Suzuki-Miyaura cross-coupling/dehydrobromination of 1, 1-dibromoalkenes to alkynes with a cyclobutene-1, 2-diylbis (imidazolium) salt as catalyst precursor.
Rahimi A and Schmidt A.
Synthesis, 2010(15), 2621-2625 (2010)
2?-[(5-Chloro-1H-indol-3-yl) methylene]-2-(1H-indol-3-yl) acetohydrazide.
Ali HM, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(4), o1807-o1808 (2007)
Kamaleddin Haj Mohammad Ebrahim Tehrani et al.
Iranian journal of pharmaceutical research : IJPR, 14(4), 1077-1086 (2015-12-15)
A series of indole-based aryl(aroyl)hydrazone analogs of antiplatelet indole-3-carboxaldehyde phenylhydrazone were synthesized by the Schiff base formation reaction and their antiplatelet activity was assessed using human platelet rich plasma. The platelet concentrate was obtained using a two-step centrifugation protocol and
Ming-Zhi Zhang et al.
European journal of medicinal chemistry, 92, 776-783 (2015-01-31)
Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp, is an indole natural products with a variety of biological activities. Based on the methods developed for the synthesis of
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