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Home > Encyclopedia > 2-Methylindoline

2-Methylindoline

2-Methylindoline structure

2-Methylindoline 

structure
  • CAS No:

    6872-06-6

  • Formula:

    C9H11N

  • Chemical Name:

    2-Methylindoline

  • Synonyms:

    1H-Indole,2,3-dihydro-2-methyl-;Indoline,2-methyl-;2,3-Dihydro-2-methyl-1H-indole;2-Methylindoline;2-Methyl-2,3-dihydroindole;2,3-Dihydro-2-methylindole;α-Methyldihydroindole;NSC 65598;2-Methyl-2,3-dihydro-1H-indole;2-Methyl-1H-indoline;(±)-2-Methylindoline;138380-84-4

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

CLEAR YELLOW TO BROWN LIQUID


2-Methylindoline is a member of indoles.

2-Methylindoline Basic Attributes

133.19

133.19

229-971-0

65598

2933990090

Characteristics

12

2.4

Clear yellow to brown Liquid

1.023 g/mL at 25 °C(lit.)

60.0-61.0 °C

115-117 °C

200 °F

n20/D 1.569(lit.)

H2O: negligible soluble

Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Safety Information

NONH for all modes of transport

3

36/37/38-52/53-22

26-36/37/39-60-57

NM1926350

Xi,Xn

Irritant

Stable under normal temperatures and pressures.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H302 (27.59%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 74 companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Methylindoline Use and Manufacturing

Methods of Manufacturing

From the hydrogenation of 2-methylindole. Heat a mixture of 130 parts of 2-methylindole, 100 parts of water and zinc amalgam (made from 196 parts of zinc) to 90°C, add 626 parts of concentrated hydrochloric acid within 30 minutes, and heat at 90-100°C for 90 minutes, Sodium hydroxide solution was added to make it alkaline, distilled, and the distillate was extracted with benzene. 2-methyl indoline was obtained.

Uses

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

1H-Indole, 2,3-dihydro-2-methyl-: INACTIVE

Computed Properties

Molecular Weight:133.19
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:133.089149355
Monoisotopic Mass:133.089149355
Topological Polar Surface Area:12
Heavy Atom Count:10
Complexity:122
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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