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2,3-DICHLOROBENZYL ALCOHOL

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2,3-DICHLOROBENZYL ALCOHOL Basic information

Product Name:
2,3-DICHLOROBENZYL ALCOHOL
Synonyms:
  • RARECHEM AL BD 0205
  • 2,3-DICHLOROBENZYL ALCOHOL
  • 2,3-DICHLOROBENZYL ALCOHOL 99%
  • Dichlorobenzylalcohol
  • 2,3-Dichlorobenzyl alcohol,99%
  • 2,3-dichloroBenzenemethanol
  • 2,3-DichlorobenzylAlcohol>
  • Benzenemethanol, 2,3-dichloro-
CAS:
38594-42-2
MF:
C7H6Cl2O
MW:
177.03
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
Mol File:
38594-42-2.mol
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2,3-DICHLOROBENZYL ALCOHOL Chemical Properties

Melting point:
85-88 °C(lit.)
Boiling point:
271.2±25.0 °C(Predicted)
Density 
1.392±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
13.69±0.10(Predicted)
color 
White to Almost white
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29062990

MSDS

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2,3-DICHLOROBENZYL ALCOHOL Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

2,3-Dichlorobenzyl alcohol may be used in the preparation of methyl [2,3-dichlorobenzyl 4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-5-(2-nitrophenylsulfonamido)-D-glycero-α-D-galacto-2-nonulopyranosid]onate and methyl [2,3-dichlorobenzyl 5-acetamido-4,7,8-tri-O-acetyl-3,5,9-trideoxy-9-(4-phenylbenzamido)-D-glycero-α-D-galacto-2-nonulopyranosid]onate.

General Description

2,3-Dichlorobenzyl alcohol is also referred to as (2,3-dichlorophenyl)methanol (IUPAC name). It is mildly antiseptic in nature.

Synthesis

6334-18-5

38594-42-2

1. To a solution of 2,3-dichlorobenzaldehyde (500 g, 2.85 mol) in methanol (3.5 L) was slowly added an alkaline solution of sodium borohydride (113.5 g, 2.975 mol) dissolved in 0.2 N sodium hydroxide solution (241 mL) at 0°C. The addition process lasted for 1 hour. The reaction mixture was stirred at room temperature for 2 hours. Subsequently, the reaction mixture was quenched by slowly pouring it into water (3.7 L) and the pH was adjusted to 6 with glacial acetic acid (125 mL). the precipitated white solid was collected by filtration to afford 2,3-dichlorobenzyl alcohol (467 g, 92% yield).

References

[1] European Journal of Medicinal Chemistry, 2016, vol. 108, p. 564 - 576
[2] Patent: US6124308, 2000, A
[3] Journal of Medicinal Chemistry, 1981, vol. 24, # 4, p. 382 - 389
[4] Organic and Biomolecular Chemistry, 2014, vol. 12, # 30, p. 5781 - 5788

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