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1-(tert-Butoxycarbonyl)-5-methylindole_Molecular_structure_CAS_129822-49-7)
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1-(tert-Butoxycarbonyl)-5-methylindole

Catalog No. 636479 Name Sigma Aldrich
CAS Number 129822-49-7 Website http://www.sigmaaldrich.com
M. F. C14H17NO2 Telephone 1-800-521-8956
M. W. 231.29028 Fax
Purity 97% Email
Storage Chembase ID: 142095

SYNONYMS

Title
1-(叔丁氧基羰基)-5-甲基吲哚
IUPAC name
tert-butyl 5-methyl-1H-indole-1-carboxylate
IUPAC Traditional name
tert-butyl 5-methylindole-1-carboxylate
Synonyms
tert-Butyl 5-methylindole-1-carboxylate

DATABASE IDS

MDL Number MFCD06008299
PubChem SID 24882785
CAS Number 129822-49-7

PROPERTIES

Empirical Formula (Hill Notation) C14H17NO2
Purity 97%
Boiling Point 208-209 °C(lit.)
Density 1.056 g/mL at 25 °C(lit.)
Flash Point >110 °C
Flash Point >230 °F
Refractive Index n20/D 1.5410(lit.)
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H317
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P280-P301 + P310
RID/ADR UN 2811 6.1/PG 3
Risk Statements 22-43
Safety Statements 36/37
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted dihydroindole derivatives via palladium-catalyzed stereoselective carboaminoxylation reactions
• Reactant in conversion of 1-Boc-indoles to 1-Boc-oxindoles
• Reactant in preparation of indolyl aromatic chiral alpha-sulfoxides
• Reactant in preparation of (indolyl)borates, silanes, and silanols
Description (简体中文)
包装
5 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted dihydroindole derivatives via palladium-catalyzed stereoselective carboaminoxylation reactions
• Reactant in conversion of 1-Boc-indoles to 1-Boc-oxindoles
• Reactant in preparation of indolyl aromatic chiral alpha-sulfoxides
• Reactant in preparation of (indolyl)borates, silanes, and silanols

REFERENCES