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Home > Encyclopedia > 2,3-Difluorobenzyl alcohol

2,3-Difluorobenzyl alcohol

2,3-Difluorobenzyl alcohol structure

2,3-Difluorobenzyl alcohol 

structure
  • CAS No:

    75853-18-8

  • Formula:

    C7H6F2O

  • Chemical Name:

    2,3-Difluorobenzyl alcohol

  • Synonyms:

    Benzenemethanol,2,3-difluoro-;2,3-Difluorobenzenemethanol;2,3-Difluorobenzyl alcohol;(2,3-Difluorophenyl)methanol

  • Categories:

    Organic Chemistry  >  Organic Fluorine Compound

Description

Clear colorless to pale brown liquid


2,3-difluorobenzyl alcohol is a member of the class of benzyl alcohols that is benzyl alcohol substituted by fluoro groups at positions 2 and 3 respectively. It is an organofluorine compound and a member of benzyl alcohols.

2,3-Difluorobenzyl alcohol Basic Attributes

144.12

144.12

7089243

922-760-0

I14VR7T96O

DTXSID70332244

2906299090

Characteristics

20.2

1.2

Clear colorless to pale brown Liquid

1.3±0.1 g/cm3

201 °F

1.497

Slightly soluble in water.

Safety Information

IRRITANT

NONH for all modes of transport

3

41-36/37/38

26-39-37/39

Xi

Irritant

P280-P305 + P351 + P338

H318

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 4 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Danger|H315 (11.63%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P310, P321, P332+P313, P337+P313, and P362|Aggregated GHS information provided by 44 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2,3-Difluorobenzyl alcohol Use and Manufacturing

Step 1 (MW-Si):Sodium borohydride (5.3 g, 140.84 mmol) was slowly added in 3 equal portions (over 25 mm)to a solution of 2, 3-difluorobenzaldehyde (20 g, 140.84 mmol) in methanol (200 mL) at 0°C.Due to the exothermic reaction the temperature raised up to ‘50°C. The reaction mixturewas stirred for 1 h and the solvent was evaporated under reduced pressure. Ethyl acetateand thereafter saturated ammonium chloride solution was added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed successively with water, brine; dried over anhydrous sodium sulfate and concentrated in vacuum to afford 20 g of MW-Si as a colorless liquid, further used withoutany purification.In a 5 ml quartz glass reaction tube, 0.1 mmol of

Computed Properties

Molecular Weight:144.12
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:144.03867113
Monoisotopic Mass:144.03867113
Topological Polar Surface Area:20.2
Heavy Atom Count:10
Complexity:108
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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