Indole-5-carboxaldehyde

• Catalog No.: 513830
• CAS Number: 1196-69-6
• M. F.: C9H7NO
• M. W.: 145.15798
• Purity: 98%

SYNONYMS

• Title: 吲哚-5-甲醛
• IUPAC name: 1H-indole-5-carbaldehyde
• IUPAC Traditional name: 1H-indole-5-carbaldehyde
• Synonyms: 5-Formylindole

DATABASE IDS

• PubChem SID: 24873717
• CAS Number: 1196-69-6
• MDL Number: MFCD02093664

PROPERTIES

• Empirical Formula (Hill Notation): C9H7NO
• Purity: 98%
• Melting Point: 100-103 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36/37/39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in poly bottle
Application

• Reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents1
• Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors2
• Reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes3
• Reactant in synthesis of para-para stilbenophanes by McMurry coupling4
• Reactant in stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes5
• Reactant in structure-based drug design of aurora kinase A inhibitors6

Description (简体中文)

包装
5 g in poly bottle
Application

• Reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents1
• Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors2
• Reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes3
• Reactant in synthesis of para-para stilbenophanes by McMurry coupling4
• Reactant in stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes5
• Reactant in structure-based drug design of aurora kinase A inhibitors6