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(4-Chloro-3-Methoxyphenyl)Methanol

Product Name
(4-Chloro-3-Methoxyphenyl)Methanol
CAS No.
13726-17-5
Chemical Name
(4-Chloro-3-Methoxyphenyl)Methanol
Synonyms
4-Chloro-3-methoxybenzyl alcohol;(4-Chloro-3-Methoxyphenyl)Methanol;Benzenemethanol, 4-chloro-3-methoxy-
CBNumber
CB92660959
Molecular Formula
C8H9ClO2
Formula Weight
172.61
MOL File
13726-17-5.mol
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(4-Chloro-3-Methoxyphenyl)Methanol Property

Boiling point:
279.2±25.0 °C(Predicted)
Density 
1.239±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
14.04±0.10(Predicted)
Appearance
White to off-white Solid
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Safety

HS Code 
2909498090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C372118
Product name
(4-chloro-3-methoxyphenyl)methanol
Packaging
25g
Price
$75
Updated
2021/12/16
TRC
Product number
C372118
Product name
(4-chloro-3-methoxyphenyl)methanol
Packaging
2.5g
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139974
Product name
(4-Chloro-3-methoxyphenyl)methanol
Packaging
500mg
Price
$70
Updated
2021/12/16
AK Scientific
Product number
J96742
Product name
(4-Chloro-3-methoxyphenyl)methanol
Packaging
5g
Price
$277
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139974
Product name
(4-Chloro-3-methoxyphenyl)methanol
Packaging
5G
Price
$431
Updated
2021/12/16
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(4-Chloro-3-Methoxyphenyl)Methanol Chemical Properties,Usage,Production

Synthesis Reference(s)

Journal of Medicinal Chemistry, 32, p. 1757, 1989 DOI: 10.1021/jm00128a016

Synthesis

85740-98-3

13726-17-5

Step 1. Dissolve 4-chloro-3-methoxybenzoic acid (1.12 g, 5.98 mmol) in tetrahydrofuran (30 mL) under ice bath conditions with stirring. A tetrahydrofuran solution of 1.0 M lithium aluminum hydride (7.18 mL, 7.18 mmol) was slowly added over approximately 5 minutes. Ice bath conditions were maintained and stirring of the reaction mixture was continued for 2 hours. Upon completion of the reaction, the reaction was quenched by slow dropwise addition of water (0.27 mL), followed by addition of 15% aqueous sodium hydroxide solution (0.27 mL), and finally water (0.82 mL). The resulting suspension was filtered and the collected solid was washed with ethyl acetate. The filtrates were combined and concentrated under reduced pressure to give (4-chloro-3-methoxyphenyl)methanol as a colorless oil (737 mg, 71% yield). The product was characterized by 1H NMR (400 MHz, CDCl3): δ 3.92 (s, 3H), 4.67 (s, 2H), 6.87 (d, J = 7.6 Hz, 1H), 6.98 (s, 1H), 7.33 (d, J = 7.6 Hz, 1H).

References

[1] Patent: US2002/77486, 2002, A1
[2] Patent: US6906063, 2005, B2
[3] Patent: EP2314593, 2016, B1. Location in patent: Paragraph 0201
[4] Journal of Medicinal Chemistry, 1987, vol. 30, # 10, p. 1887 - 1891
[5] Journal of Medicinal Chemistry, 1992, vol. 35, # 23, p. 4408 - 4414

(4-Chloro-3-Methoxyphenyl)Methanol Preparation Products And Raw materials

Raw materials

Preparation Products

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(4-Chloro-3-Methoxyphenyl)Methanol Suppliers

Aladdin Scientific
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United States
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Synthonix Inc
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SynQuest Laboratories, Inc.
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Matrix Scientific
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Country
United States
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13726-17-5, (4-Chloro-3-Methoxyphenyl)MethanolRelated Search:


  • (4-Chloro-3-Methoxyphenyl)Methanol
  • 4-Chloro-3-methoxybenzyl alcohol
  • Benzenemethanol, 4-chloro-3-methoxy-
  • 13726-17-5