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2-Methylindoline

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2-Methylindoline Basic information

Product Name:
2-Methylindoline
Synonyms:
  • 1H-Indole, 2,3-dihydro-2-methyl-
  • 1H-Indole,2,3-dihydro-2-methyl-
  • 2,3-dihydro-2-methyl-1h-indol
  • 2,3-Dihydro-2-methyl-1H-indole
  • 2-Methyl-2,3-dihydroindole
  • 2-methyl-indolin
  • alpha-Methyldihydroindole
  • Dihydroindole, 2-methyl-
CAS:
6872-06-6
MF:
C9H11N
MW:
133.19
EINECS:
229-971-0
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • pharmacetical
  • Indoline & Oxindole
  • Heterocyclic Compounds
  • Indoles
  • Indoles and derivatives
  • Heterocycle-Indole series
  • intermediates
Mol File:
6872-06-6.mol
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2-Methylindoline Chemical Properties

Melting point:
-51 °C
Boiling point:
228-229 °C (lit.)
Density 
1.023 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.569(lit.)
Flash point:
200 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform, Methanol
form 
Liquid
pka
5.26±0.40(Predicted)
Specific Gravity
1.02
color 
Clear yellow to brown
Water Solubility 
negligible
CAS DataBase Reference
6872-06-6(CAS DataBase Reference)
NIST Chemistry Reference
2-Methylindoline(6872-06-6)
EPA Substance Registry System
1H-Indole, 2,3-dihydro-2-methyl- (6872-06-6)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-52/53-22
Safety Statements 
26-36/37/39-60-57
WGK Germany 
3
RTECS 
NM1926350
Hazard Note 
Irritant
HS Code 
29349990

MSDS

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2-Methylindoline Usage And Synthesis

Chemical Properties

CLEAR YELLOW TO BROWN LIQUID

Uses

2-Methylindoline is an intermediate in the production of various indole derivatives

Uses

Reactant for preparation of:

  • Inhibitors of NOD1-induced nuclear factor-κB activation
  • Red fluorescent dyes for organic light-emitting diodes
  • Norepinephrine reuptake inhibitors
  • MT2-selective melatonin receptor antagonists
  • Protease-activated receptor-1 antagonists
  • Diuretic agent indapamide
  • Dopamine D2/D4 receptor antagonists
  • Antitumor agents

Definition

ChEBI: 2-Methylindoline is a member of indoles.

Synthesis Reference(s)

Journal of the American Chemical Society, 111, p. 4108, 1989 DOI: 10.1021/ja00193a056
Chemical and Pharmaceutical Bulletin, 26, p. 108, 1978 DOI: 10.1248/cpb.26.108

2-Methylindoline Preparation Products And Raw materials

Preparation Products

Raw materials

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