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Home > Encyclopedia > 2,6-Di-tert-butylnaphthalene

2,6-Di-tert-butylnaphthalene

2,6-Di-tert-butylnaphthalene structure

2,6-Di-tert-butylnaphthalene 

structure
  • CAS No:

    3905-64-4

  • Formula:

    C18H24

  • Chemical Name:

    2,6-Di-tert-butylnaphthalene

  • Synonyms:

    Naphthalene,2,6-bis(1,1-dimethylethyl)-;Naphthalene,2,6-di-tert-butyl-;2,6-Bis(1,1-dimethylethyl)naphthalene;2,6-Di-tert-butylnaphthalene;NSC 91463;2,6-Di-t-butylnaphthalene;2,6-Ditert-butylnaphthalene

2,6-Di-tert-butylnaphthalene Basic Attributes

240.38

240.38

223-461-1

91463

DTXSID20192299

2902909090

Characteristics

0

5.43480

0.935 g/cm3

145-146 °C @ Solvent: Methanol

335.1ºC at 760 mmHg

165.2ºC

1.542

Safety Information

36/37/38

26-36/37/39

P264, P270, P273, P301+P312, P330, P391, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P301+P312, P330, P391, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2,6-Di-tert-butylnaphthalene Use and Manufacturing

Methods of Manufacturing

It is derived from the condensation of naphthalene and chloro-tert-butane. During the reaction, needle-like crystals of 2, 7-di-tert-butylnaphthalene [10275-58-8] were also formed.

Uses

Can be used as pharmaceutical intermediates. The two isomers do not need to be separated, sulfonated with chlorosulfonic acid, and then neutralized with sodium carbonate to obtain sodium 3,6-di-tert-butyl naphthalenesulfonate [14992-59-7] and 3,7-di-tert Sodium butylnaphthalene sulfonate, that is, non-narcotic potent antitussive drug Kening.

Computed Properties

Molecular Weight:240.4
XLogP3:6.9
Rotatable Bond Count:2
Exact Mass:240.187800766
Monoisotopic Mass:240.187800766
Heavy Atom Count:18
Complexity:245
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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