tert-Butyl indoline-1-carboxylate

• Catalog No.: 510149
• CAS Number: 143262-10-6
• M. F.: C13H17NO2
• M. W.: 219.27958
• Purity: 98%

SYNONYMS

• Title: 吲哚啉-1-羧酸叔丁酯
• IUPAC name: tert-butyl 2,3-dihydro-1H-indole-1-carboxylate
• IUPAC Traditional name: tert-butyl 2,3-dihydroindole-1-carboxylate
• Synonyms: N-(tert-Butoxycarbonyl)-2,3-dihydroindole

DATABASE IDS

• MDL Number: MFCD01318399
• PubChem SID: 24873481
• CAS Number: 143262-10-6

PROPERTIES

• Purity: 98%
• Empirical Formula (Hill Notation): C13H17NO2
• Boiling Point: 83-84 °C/0.1 mmHg(lit.)
• Flash Point: 110 °C
• Flash Point: 230 °F
• Melting Point: 46-50 °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
5, 25 g in glass bottle
Application

• Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd1
• Reactant in preparation of allyl- and arylindolines2
• Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B3
• Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions4
• Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach5

Description (简体中文)

包装
5, 25 g in glass bottle
Application

• Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd1
• Reactant in preparation of allyl- and arylindolines2
• Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B3
• Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions4
• Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach5