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N-Boc-5-methoxyindole_Molecular_structure_CAS_99275-47-5)
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N-Boc-5-methoxyindole

Catalog No. 680613 Name Sigma Aldrich
CAS Number 99275-47-5 Website http://www.sigmaaldrich.com
M. F. C14H17NO3 Telephone 1-800-521-8956
M. W. 247.28968 Fax
Purity 97% Email
Storage Chembase ID: 87802

SYNONYMS

Title
N-Boc-5-甲氧基吲哚
IUPAC name
tert-butyl 5-methoxy-1H-indole-1-carboxylate
IUPAC Traditional name
tert-butyl 5-methoxyindole-1-carboxylate
Synonyms
N-(叔丁氧羰基)-5-甲氧基吲哚
N-(tert-Butoxycarbonyl)-5-methoxyindole
5-Methoxyindole-1-carboxylic acid tert-butyl ester

DATABASE IDS

MDL Number MFCD08272248
CAS Number 99275-47-5
PubChem SID 24885580

PROPERTIES

Empirical Formula (Hill Notation) C14H17NO3
Purity 97%
Melting Point 75-79 °C
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H319
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P301 + P310-P305 + P351 + P338
RID/ADR UN 2811 6.1/PG 3
Risk Statements 22-36
Safety Statements 26
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
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
Description (简体中文)
包装
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

REFERENCES