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1-BOC-INDOLINE

Product Name
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
Formula Weight
219.28
MOL File
143262-10-6.mol
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1-BOC-INDOLINE Property

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
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
510149
Product name
tert-Butyl indoline-1-carboxylate
Purity
98%
Packaging
5g
Price
$20.2
Updated
2023/06/20
Alfa Aesar
Product number
L17477
Product name
1-Boc-indoline, 98%
Packaging
5g
Price
$40.6
Updated
2021/12/16
Alfa Aesar
Product number
L17477
Product name
1-Boc-indoline, 98%
Packaging
1g
Price
$18.2
Updated
2021/12/16
TRC
Product number
B663400
Product name
1-Boc-Indoline
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
B663400
Product name
1-Boc-Indoline
Packaging
50mg
Price
$60
Updated
2021/12/16
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1-BOC-INDOLINE Chemical Properties,Usage,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

143262-10-6, 1-BOC-INDOLINERelated Search:


  • 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