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Home > Encyclopedia > Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate

Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate

Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate structure

Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate 

structure
  • CAS No:

    10226-28-5

  • Formula:

    C9H14O3

  • Chemical Name:

    Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate

  • Synonyms:

    2H-Pyran-5-carboxylic acid,3,4-dihydro-6-methyl-,ethyl ester;Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate;2-Methyl-3-carbethoxy-5,6-dihydropyran;NSC 30277;Ethyl 6-methyl-3,4-dihydro-2H-pyran-5-carboxylate;3,4-Dihydro-6-methyl-2H-Pyran-5-carboxylic acid ethyl ester

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

Colourless Oil

Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate Basic Attributes

170.21

170.21

233-543-9

30277

DTXSID30144845

2932999099

Characteristics

35.5

1.49

1.0564 g/cm3 @ Temp: 20 °C

104-105 °C @ Press: 10 Torr

89.2±18.9 °C

1.466

0.0642mmHg at 25°C

Safety Information

3272

10

16

P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501

H226

|Warning|H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]|P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501|Aggregated GHS information provided by 157 companies from 1 notifications to the ECHA C&L Inventory.

Ethyl 3,4-dihydro-6-methyl-2H-pyran-5-carboxylate Use and Manufacturing

Methods of Manufacturing

It is obtained by condensation of 1, 3-bromochloropropane and ethyl acetoacetate in the participation of potassium carbonate.

Uses

Intermediate of pentoxifylline.

Computed Properties

Molecular Weight:170.21
XLogP3:1.5
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:170.094294304
Monoisotopic Mass:170.094294304
Topological Polar Surface Area:35.5
Heavy Atom Count:12
Complexity:206
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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