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2-(1H-Indol-2-yl)aniline

CAS No.
32566-01-1
Chemical Name:
2-(1H-Indol-2-yl)aniline
Synonyms
2-(2-AMINOPHENYL)INDOLE;2-(1H-indol-2-yl)aniline;2-(2'-AMINOPHENYL)INDOLE;2-(2-Aminophenyl)indole 97%;2-(1H-indol-2-yl)-Benzenamine;Benzenamine, 2-(1H-indol-2-yl)-
CBNumber:
CB1145700
Molecular Formula:
C14H12N2
Molecular Weight:
208.26
MDL Number:
MFCD00134432
MOL File:
32566-01-1.mol
Last updated:2022-11-11 11:01:00

2-(1H-Indol-2-yl)aniline Properties

Melting point 154-155 °C(lit.)
Boiling point 437.9±20.0 °C(Predicted)
Density 1.229±0.06 g/cm3(Predicted)
pka 16.53±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3

2-(1H-Indol-2-yl)aniline price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0001010 2-(2-AMINOPHENYL)INDOLE 95.00% 32566-01-1 1G $817.39 2021-12-16 Buy
Arctom AS030106 2-(1H-Indol-2-yl)aniline 97% 32566-01-1 1g $956 2021-12-16 Buy
Ambeed A257993 2-(1H-Indol-2-yl)aniline 97% 32566-01-1 100mg $83 2021-12-16 Buy
Ambeed A257993 2-(1H-Indol-2-yl)aniline 97% 32566-01-1 250mg $124 2021-12-16 Buy
Arctom AS030106 2-(1H-Indol-2-yl)aniline 97% 32566-01-1 100mg $255 2021-12-16 Buy
Product number Packaging Price Buy
API0001010 1G $817.39 Buy
AS030106 1g $956 Buy
A257993 100mg $83 Buy
A257993 250mg $124 Buy
AS030106 100mg $255 Buy

2-(1H-Indol-2-yl)aniline Chemical Properties,Uses,Production

Uses

Reactant in:

  • cascade reactions of benzopyranylidenemalonates with mono- and dinucleophiles

Reactant for preparation of:
  • Mono-, bis-indolo[1,2-c]quinazolines as antimicrobial agents
  • Isocryptolepine alkaloid with antimalarial activity
  • Cyanoindolo[3,2-c]quinolines and benzimidazo[1,2-c]quinazolines as antitumor agents

General Description

2-(2-Aminophenyl)indole is an indole derivative. It has been reported as an amination reagent. 2-(2-Aminophenyl)indole undergoes condensation with 4,5-dichloro-1,2,3-dithiazolium chloride (Appel salt) to afford new 6-cyanoindolo[3,2-c]quinoline derivatives, having pharmacological applications.

2-(1H-Indol-2-yl)aniline Preparation Products And Raw materials

Raw materials

Preparation Products

2-(1H-Indol-2-yl)aniline Suppliers

Global( 37)Suppliers
Supplier Tel Email Country ProdList Advantage
Hefei Hirisun Pharmatech Co., Ltd
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Coresyn Pharmatech Co., Ltd.
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PT CHEM GROUP LIMITED
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GIHI CHEMICALS CO.,LIMITED
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Amadis Chemical Company Limited
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Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696; info@hanhongsci.com China 42982 64
ShangHai AmK Pharmaceutical Technology Co., Ltd. 18019252918 sale@amkchem.com China 15415 55
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-0755-85201366 18938635012 sales@regentsciences.com China 9287 58
2-(2'-AMINOPHENYL)INDOLE 2-(2-AMINOPHENYL)INDOLE 2-(2-Aminophenyl)indole 97% 2-(1H-indol-2-yl)-Benzenamine Benzenamine, 2-(1H-indol-2-yl)- 2-(1H-indol-2-yl)aniline 32566-01-1 Indoles Heterocyclic Building Blocks Building Blocks Intermediates of Dyes and Pigments Building Blocks Heterocyclic Building Blocks Indoles