Substance
ID:318261
Names and Identifiers
IUPAC Traditional name
tert-butyl 5-methoxyindole-1-carboxylate
IUPAC name
tert-butyl 5-methoxy-1H-indole-1-carboxylate
Synonyms
N-(tert-Butoxycarbonyl)-5-methoxyindole5-Methoxyindole-1-carboxylic acid tert-butyl esterN-(叔丁氧羰基)-5-甲氧基吲哚N-Boc-5-甲氧基吲哚N-Boc-5-methoxyindole
Properties
Safety Information
MSDS Link
RID/ADR
UN 2811 6.1/PG 3
European Hazard Symbols
Harmful (Xn)German water hazard class
3
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Signal Word
Danger
Packing Group
3
Hazard Class
6.1
UN Number
2811
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements
P301+P310-P305+P351+P338
Risk Statements
22-36
GHS Hazard statements
H301-H319
Safety Statements
26
Physical Property
Melting Point
75-79 °C
Product Information
Empirical Formula (Hill Notation)
C14H17NO3
Purity
97%
Molecule Details
Packaging
1, 10 g in glass bottle
Application
Reactant for preparation of:
• Asymmetric intramolecular Friedel-Crafts alkylation reaction1
• Palladium-catalyzed carboaminoxylations with arylboronic acids and TEMPO catalyst2
• Fluorescent pyrimidopyrimidoindole nucleosides via Suzuki-Miyaura coupling reaction3
• Novel conformationally restricted β- and γ-amino acids4
• 2-(Indolyl) borates, silanes, and silanols5
• DNA minor groove alkylating agents as stable amine-based prodrugs designed for tumor-specific release6
1, 10 g in glass bottle
Application
Reactant for preparation of:
• Asymmetric intramolecular Friedel-Crafts alkylation reaction1
• Palladium-catalyzed carboaminoxylations with arylboronic acids and TEMPO catalyst2
• Fluorescent pyrimidopyrimidoindole nucleosides via Suzuki-Miyaura coupling reaction3
• Novel conformationally restricted β- and γ-amino acids4
• 2-(Indolyl) borates, silanes, and silanols5
• DNA minor groove alkylating agents as stable amine-based prodrugs designed for tumor-specific release6
Molecular Spectra
No Data Available
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References
No Data Available
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