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1-BOC-INDOLINE

CAS No.
143262-10-6
Chemical Name:
1-BOC-INDOLINE
Synonyms
1-BOC-INDOLINE;BUTTPARK 52\06-71;1-(tert-Butoxycarbonyl)indoline;TERT-BUTYL INDOLINE-1-CARBOXYLATE;N-(tert-Butoxycarbonyl)-2,3-dihydroindole;tert-butyl 2,3-dihydroindole-1-carboxylate;2,3-dihydroindole-1-carboxylic acid tert-butyl ester;1H-Indole-1-carboxylic acid, 2,3-dihydro-, 1,1-diMethylethyl ester
CBNumber:
CB2169468
Molecular Formula:
C13H17NO2
Molecular Weight:
219.28
MDL Number:
MFCD01318399
MOL File:
143262-10-6.mol
Last updated:2023-07-14 17:31:15

1-BOC-INDOLINE Properties

Melting point 46-50 °C(lit.)
Boiling point 83-84 °C0.1 mm Hg(lit.)
Density 1.114±0.06 g/cm3(Predicted)
Flash point >230 °F
pka 0.84±0.20(Predicted)
BRN 5336249
CAS DataBase Reference 143262-10-6

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
NFPA 704
1
2 0

1-BOC-INDOLINE price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 510149 tert-Butyl indoline-1-carboxylate 98% 143262-10-6 5g $20.2 2023-06-20 Buy
Alfa Aesar L17477 1-Boc-indoline, 98% 143262-10-6 5g $40.6 2021-12-16 Buy
Alfa Aesar L17477 1-Boc-indoline, 98% 143262-10-6 1g $18.2 2021-12-16 Buy
TRC B663400 1-Boc-Indoline 143262-10-6 10mg $45 2021-12-16 Buy
TRC B663400 1-Boc-Indoline 143262-10-6 50mg $60 2021-12-16 Buy
Product number Packaging Price Buy
510149 5g $20.2 Buy
L17477 5g $40.6 Buy
L17477 1g $18.2 Buy
B663400 10mg $45 Buy
B663400 50mg $60 Buy

1-BOC-INDOLINE Chemical Properties,Uses,Production

Uses

Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd 1 Reactant in preparation of allyl- and arylindolines 2 Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B 3 Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions 4 Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach.

Uses

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

General Description

tert -Butyl indoline-1-carboxylate is an N-substituted indoline derivative.

1-BOC-INDOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 43)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Nextpeptide Inc
+86-0571-81612335 +8613336028439 sales@nextpeptide.com China 19915 58
Sichuan Biosynce Pharmatech Co., Ltd.
+8619950309693 diane@biosynce.com China 4874 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006608290; 18621169109 market03@meryer.com China 40241 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30132 84
Energy Chemical 021-021-58432009 400-005-6266 sales8178@energy-chemical.com China 44751 61
Adamas Reagent, Ltd. 400-6009262 16621234537 zhangsn@titansci.com China 14113 59

1-BOC-INDOLINE Spectrum

BUTTPARK 52\06-71 1-BOC-INDOLINE TERT-BUTYL INDOLINE-1-CARBOXYLATE 1H-Indole-1-carboxylic acid, 2,3-dihydro-, 1,1-diMethylethyl ester N-(tert-Butoxycarbonyl)-2,3-dihydroindole 1-(tert-Butoxycarbonyl)indoline 2,3-dihydroindole-1-carboxylic acid tert-butyl ester tert-butyl 2,3-dihydroindole-1-carboxylate 143262-10-6 Heterocyclic Building Blocks Indoles Building Blocks Building Blocks Heterocyclic Building Blocks Indoles Heterocyclic Compounds