4-Hydroxyindole

• Catalog No.: 219878
• CAS Number: 2380-94-1
• M. F.: C8H7NO
• M. W.: 133.14728
• Purity: 99%

SYNONYMS

• Title: 对羟基吲哚
• IUPAC name: 1H-indol-4-ol
• IUPAC Traditional name: hydroxyindole
• Synonyms: 4-Indolol; 4-羟基吲哚; 对羟基吲哚; 4-Hydroxyindole

DATABASE IDS

• Beilstein Number: 114905
• MDL Number: MFCD00005667
• EC Number: 219-177-2
• PubChem SID: 24853151
• CAS Number: 2380-94-1

PROPERTIES

• Empirical Formula (Hill Notation): C8H7NO
• Purity: 99%
• Melting Point: 97-99 °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
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
250 mg in glass bottle
Application

• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes1
• Reactant for preparation of small molecules targeting interaction between HIV-1 integrase and LEDGF/p75 cofactor2
• Reactant for preparation of dopamine D2 receptor antagonists3
• Reactant for preparation of SCD inhibitor MF-4384
• Reactant for preparation of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer5
• Reactant for preparation of indole/quinoline carbothioic acid amide derivatives as HCV inhibitors6

Description (简体中文)

包装
1 g in glass bottle
250 mg in glass bottle
Application

• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes1
• Reactant for preparation of small molecules targeting interaction between HIV-1 integrase and LEDGF/p75 cofactor2
• Reactant for preparation of dopamine D2 receptor antagonists3
• Reactant for preparation of SCD inhibitor MF-4384
• Reactant for preparation of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer5
• Reactant for preparation of indole/quinoline carbothioic acid amide derivatives as HCV inhibitors6