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5-Hydroxyindole

Catalog No. H31859 Name Sigma Aldrich
CAS Number 1953-54-4 Website http://www.sigmaaldrich.com
M. F. C8H7NO Telephone 1-800-521-8956
M. W. 133.14728 Fax
Purity 97% Email
Storage Chembase ID: 15934

SYNONYMS

Title
5-羟基苯并吡咯
IUPAC name
1H-indol-5-ol
IUPAC Traditional name
5-hydroxyindol
Synonyms
5-Indolol
5-Hydroxyindole
5-羟基吲哚
NSC 87503
5-羟基苯并吡咯

DATABASE IDS

Beilstein Number 112349
PubChem SID 24895561
MDL Number MFCD00005677
EC Number 217-782-6
CAS Number 1953-54-4

PROPERTIES

Empirical Formula (Hill Notation) C8H7NO
Purity 97%
Melting Point 106-108 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
RTECS NM2430000
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
Application

• Reactant for preparation of (oxoimidazolidinyl/oxopyrimidinyl)benzenesulfonates as antitumor agents and tubulin inhibitors1
• Reactant for preparation of anthranilic acids2
• Reactant for preparation of indole compounds as dopamine D2 receptor antagonists3
• Reactant for preparation of naphthalimide- or carbazole-containing human β-adrenoceptor ligands4
• Reactant for preparation of melanins as nature-inspired radioprotectors5
• Reactant for preparation of 5-vinyl-3-pyridinecarbonitriles as PKCθ inhibitors6
Description (简体中文)
包装
1 g in glass bottle
Application

• Reactant for preparation of (oxoimidazolidinyl/oxopyrimidinyl)benzenesulfonates as antitumor agents and tubulin inhibitors1
• Reactant for preparation of anthranilic acids2
• Reactant for preparation of indole compounds as dopamine D2 receptor antagonists3
• Reactant for preparation of naphthalimide- or carbazole-containing human β-adrenoceptor ligands4
• Reactant for preparation of melanins as nature-inspired radioprotectors5
• Reactant for preparation of 5-vinyl-3-pyridinecarbonitriles as PKCθ inhibitors6

REFERENCES