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Home > Encyclopedia > 2,4-Dichloro-5-(1-methylethoxy)benzenamine

2,4-Dichloro-5-(1-methylethoxy)benzenamine

2,4-Dichloro-5-(1-methylethoxy)benzenamine structure

2,4-Dichloro-5-(1-methylethoxy)benzenamine 

structure
  • CAS No:

    41200-96-8

  • Formula:

    C9H11Cl2NO

  • Chemical Name:

    2,4-Dichloro-5-(1-methylethoxy)benzenamine

  • Synonyms:

    Benzenamine,2,4-dichloro-5-(1-methylethoxy)-;2,4-Dichloro-5-(1-methylethoxy)benzenamine;2,4-Dichloro-5-isopropoxyaniline;2,4-Dichloro-5-isopropoxyphenylamine;2,4-Dichloro-5-(propan-2-yloxy)aniline;2,4-Dichloro-5-propan-2-yloxyaniline

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

2,4-Dichloro-5-(1-methylethoxy)benzenamine Basic Attributes

220.1

220.10

2836827

255-258-9

DTXSID90194124

2922299090

Characteristics

35.2

3.94400

1.272g/cm3

40-42°C

102 °C @ Press: 0.1 Torr

110-112°C/0.2mm

1.562

Safety Information

III

6.1

2811

20/21/22

28-36/37

Xi

Irritant

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P332+P313, P362, P363, P403+P233, P405, P501

H302+H312

|Danger|H302+H312 (96.19%): Harmful if swallowed or in contact with skin [Warning Acute toxicity, oral; acute toxicity, dermal]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P332+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 105 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2,4-Dichloro-5-(1-methylethoxy)benzenamine Use and Manufacturing

Methods of Manufacturing

The preparation method is to add 2, 4-dichloro-5-isopropoxynitrobenzene, hydrogenation catalyst, auxiliary agent and methanol into the reaction kettle, replace the air in the kettle with hydrogen 3 times, and maintain the hydrogen pressure in the kettle Start stirring at 2.0 MPa, keep the hydrogen pressure at 2.0 MPa at an appropriate temperature, add hydrogen for several hours until the reaction no longer absorbs hydrogen, take a sample and check, the reaction is over, stop stirring, let stand for a period of time, release the pressure, and press out the material Then, it is filtered to remove the catalyst, and then desolventize under reduced pressure to obtain the product.

Uses

2,4-Dichloro-5-isopropoxyaniline is an intermediate of the herbicide oxadiazon.

Computed Properties

Molecular Weight:220.09
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:219.0217694
Monoisotopic Mass:219.0217694
Topological Polar Surface Area:35.2
Heavy Atom Count:13
Complexity:166
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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