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4-Methoxybenzylchloride

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4-Methoxybenzylchloride Basic information

Product Name:
4-Methoxybenzylchloride
Synonyms:
  • P-METHOXYBENZYL CHLORIDE
  • alpha-Chloro-4-methoxytoluene
  • Anisole, p-(chloromethyl)-
  • Benzene, 1-(chloromethyl)-4-methoxy-
  • p-(Chloromethyl)anisole
  • p-Anisyl chloride
  • 4-Methoxybenzylchloride, stabilized, 98% 5GR
  • Anisyl Chloride 4-(Chloromethyl)anisole
CAS:
824-94-2
MF:
C8H9ClO
MW:
156.61
EINECS:
212-540-6
Product Categories:
  • Biochemistry
  • Reagents for Oligosaccharide Synthesis
  • alkyl chloride
Mol File:
824-94-2.mol
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4-Methoxybenzylchloride Chemical Properties

Melting point:
−1 °C(lit.)
Boiling point:
117-118 °C14 mm Hg(lit.)
Density 
1.155 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.548(lit.)
Flash point:
229 °F
storage temp. 
Inert atmosphere,2-8°C
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Liquid
color 
Clear colorless to pale yellow
Water Solubility 
slowly decomposes
Stability:
Moisture Sensitive
InChIKey
MOHYOXXOKFQHDC-UHFFFAOYSA-N
CAS DataBase Reference
824-94-2(CAS DataBase Reference)
NIST Chemistry Reference
«alpha»-Chloro-4-methoxytoluene(824-94-2)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-27-36/37/39-45
RIDADR 
UN 3265 8/PG 3
WGK Germany 
3
10-19-21
Autoignition Temperature
109℃
Hazard Note 
Corrosive
TSCA 
No
HazardClass 
8
PackingGroup 
III
HS Code 
29093090

MSDS

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4-Methoxybenzylchloride Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

O/N protecting group reagent which can be mildly oxidatively cleaved, e.g., with ceric ammonium nitrate.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 20, p. 190, 1977 DOI: 10.1021/jm00212a002
The Journal of Organic Chemistry, 53, p. 3634, 1988 DOI: 10.1021/jo00250a048

General Description

4-Methoxybenzyl chloride undergoes mild oxidative claevage with ceric ammonium nitrate.

Purification Methods

Purify 4-anisyl chloride by fractional distillation under vacuum, and the middle fraction is redistilled at 10-6 mm at room temperature by intermittent cooling of the receiver in liquid N2, and the middle fraction is collected. [Mohammed & Kosower J Am Chem Soc 93 2709 1971, Beilstein 6 IV 2137.]

4-Methoxybenzylchloride Preparation Products And Raw materials

Preparation Products

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