ChemicalBook > Product Catalog >Organic Chemistry >Aldehydes >Indole-5-carboxaldehyde

Indole-5-carboxaldehyde

Indole-5-carboxaldehyde Structure
CAS No.
1196-69-6
Chemical Name:
Indole-5-carboxaldehyde
Synonyms
1H-INDOLE-5-CARBALDEHYDE;CL092;e-5-carboxaL;5-FORMYLINDOLE;5-INDOLE ALDEHYDE;INDOLE-5-ALDEHYDE;5-Formyl-1H-indole;INDOLE-5-CARBALDEHYDE;Indole-5-Carboxadehyde;1H-indol-5-carbaldehyde
CBNumber:
CB0155236
Molecular Formula:
C9H7NO
Molecular Weight:
145.16
MOL File:
1196-69-6.mol
Modify Date:
2024/7/30 16:49:16

Indole-5-carboxaldehyde Properties

Melting point 100-103 °C(lit.)
Boiling point 339.1±15.0 °C(Predicted)
Density 1.278±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO, Methanol
form Powder
pka 16.14±0.30(Predicted)
color Orange or tan
Water Solubility Insoluble in water.
Sensitive Air Sensitive
CAS DataBase Reference 1196-69-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
Hazard Note  Irritant/Keep Cold
HazardClass  IRRITANT
HS Code  29339900
NFPA 704
1
2 1

Indole-5-carboxaldehyde price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 513830 Indole-5-carboxaldehyde 98% 1196-69-6 5G ₹15858.63 2022-06-14 Buy
TCI Chemicals (India) I0674 Indole-5-carboxaldehyde min. 98.0 % 1196-69-6 5G ₹10700 2022-05-26 Buy
TCI Chemicals (India) I0674 Indole-5-carboxaldehyde min. 98.0 % 1196-69-6 25G ₹32800 2022-05-26 Buy
Product number Packaging Price Buy
513830 5G ₹15858.63 Buy
I0674 5G ₹10700 Buy
I0674 25G ₹32800 Buy

Indole-5-carboxaldehyde Chemical Properties,Uses,Production

Chemical Properties

Red Crystalline Powder

Uses

Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes and in structure-based drug design of aurora kinase A inhibitors.

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1H-indol-5-carbaldehyde 1H-INDOLE-5-CARBOXALDEHYDE 5-INDOLE ALDEHYDE 5-FORMYLINDOLE INDOLE-5-CARBALDEHYDE INDOLE-5-ALDEHYDE INDOLE-5-CARBOXALDEHYDE 5-Formyl-1H-indole 1H-Indole-5-carboxaldehyde (9CI) INDOLE-5-CARBOXYALDEHYDE INDOLE-5-CARBOXALDEHYDE (5-FORMYLINDOLE) Indole-5-Carboxadehyde 1H-INDOLE-5-CARBALDEHYDEINDOLE-5-CARBOXALDEHYDE INDOLE-5-CARBOXALDEHYDE, 98+% 1H-indole-5-carbaldehyde(SALTDATA: FREE) H-Indole-5-carboxaldehyde CL092 1H-Indole-5-carboxaldehyde 99% Indole-5-carboxaldehyde in stock Factory Indole-5-carboxaldehyde> e-5-carboxaL Indole-5-carboxaldehyde ISO 9001:2015 REACH 1H-INDOLE-5-CARBALDEHYDE Indole-5-carboxaldehyde (7CI, 8CI) 1196-69-6 1196-69-8 1196-89-6 196-69-6 ALDEHYDE Indoles Heterocyclic Building Blocks Building Blocks Simple Indoles Building Blocks Heterocyclic Building Blocks Building Blocks Indole Derivatives Indole Indoles Indoles and derivatives ALDEHYDE Aldehydes blocks IndolesOxindoles Heterocycle-Indole series