Passa al contenuto
Merck
Tutte le immagini(1)

Key Documents

View All Documentation

533076

Sigma-Aldrich

5-Chloroindole-3-carboxaldehyde

98%

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C9H6ClNO
Numero CAS:
827-01-0
Peso molecolare:
179.60
Numero MDL:
MFCD00175291
Codice UNSPSC:
12352100
ID PubChem:
24877937

Saggio

98%

Punto di fusione

213-216 °C (lit.)

Gruppo funzionale

aldehyde
chloro

Stringa SMILE

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
YXEXOIGXNYITQH-UHFFFAOYSA-N

Descrizione generale

5-Chloroindole-3-carboxaldehyde, also known as 5-chloro-1H-indole-3-carboxaldehyde, is an indole derivative.

Applicazioni

5-Chloroindole-3-carboxaldehyde (5-Chloro-1H-indole-3-carboxaldehyde) may be used in the preparation of:
  • 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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
MKBW3434V
MKBC9142V
MKBC9142
MKBD3116
MKBC9301

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

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

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.