1H-Indole-4-carbaldehyde

Modify Date: 2025-08-20 19:08:00

1H-Indole-4-carbaldehyde Structure
1H-Indole-4-carbaldehyde structure
Common Name 1H-Indole-4-carbaldehyde
CAS Number 1074-86-8 Molecular Weight 145.16
Density 1.3±0.1 g/cm3 Boiling Point 339.1±15.0 °C at 760 mmHg
Molecular Formula C9H7NO Melting Point 139-143 °C(lit.)
MSDS Chinese USA Flash Point 166.8±27.8 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 1H-Indole-4-carbaldehyde


1H-Indole-4-carbaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name Indole-4-carboxaldehyde
Synonym More Synonyms

 1H-Indole-4-carbaldehyde Biological Activity

Description 1H-Indole-4-carbaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro Indole-4-carboxaldehyde 是一种合成中间体,可用于药物合成。

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 339.1±15.0 °C at 760 mmHg
Melting Point 139-143 °C(lit.)
Molecular Formula C9H7NO
Molecular Weight 145.16
Flash Point 166.8±27.8 °C
Exact Mass 145.052765
PSA 32.86000
LogP 1.56
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.729
InChIKey JFDDFGLNZWNJTK-UHFFFAOYSA-N
SMILES O=Cc1cccc2[nH]ccc12
Storage condition Keep Cold

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H317-H319
Precautionary Statements P280-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes Xn:Harmful
Risk Phrases R22;R36;R43
Safety Phrases S26-S36/37
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Synthetic Route

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles6

More Articles
One-pot synthesis of 2-substituted indoles from 2-aminobenzyl phosphonium salts. A formal total synthesis of arcyriacyanin A.

Org. Lett. 10(14) , 3061-3, (2008)

The reaction of (2-aminobenzyl) triphenylphosphonium bromide with aromatic aldehydes or alpha,beta-unsaturated aldehydes under microwave-assisted conditions constitutes a new synthesis of 2-substitute...

Synthesis and biological evaluation of achiral indole-substituted titanocene dichloride derivatives.

Int J Med Chem 2012 , 905981, (2015)

Six new titanocene compounds have been isolated and characterised. These compounds were synthesised from their fulvene precursors using Super Hydride (LiBEt3H) followed by transmetallation with titani...

A New Synthesis method of indole-4-carboxaldehyde. Wu Y-M, et al.

Chinese J. Synth. Chem. 12 , 333-35, (2004)

 Synonyms

Indole-4-Carboxaldehyde
MFCD01632221
4-Indole-carboxaldehyde
4-Formylindole
1H-Indole-4-carbaldehyde
1H-Indole-4-carboxaldehyde
4-Indolecarbaldehyde
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