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4-(CHLOROMETHYL)BENZYL ALCOHOL 99

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CAS:16473-35-1
Purity:0.99 Package:1kg; 25kg; or larger package as required
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Products Intro: Product Name:(4-Chloromethyl-phenyl)-methanol
CAS:16473-35-1
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4-(CHLOROMETHYL)BENZYL ALCOHOL 99 manufacturers

4-(CHLOROMETHYL)BENZYL ALCOHOL 99 Basic information
Product Name:4-(CHLOROMETHYL)BENZYL ALCOHOL 99
Synonyms:4-(CHLOROMETHYL)BENZYL ALCOHOL 99;BenzeneMethanol, 4-(chloroMethyl)-;1-(Chloromethyl)-4-(hydroxymethyl)benzene;4-(ChloroMethyl)benzyl alcohol;4-(ChloroMethyl)benzyl alcohol 99%;p-hydroxymethylbenzyl chloride;4-(hydroxymethyl)benzyl chloride;Plerixafor Impurity 44
CAS:16473-35-1
MF:C8H9ClO
MW:156.61
EINECS:
Product Categories:Alcohols;C7 to C8;Oxygen Compounds;16473-35-1
Mol File:16473-35-1.mol
4-(CHLOROMETHYL)BENZYL ALCOHOL  99 Structure
4-(CHLOROMETHYL)BENZYL ALCOHOL 99 Chemical Properties
Melting point 58-60 °C (lit.)
Boiling point 276℃
density 1.195
Fp 123℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka14.27±0.10(Predicted)
form wooly solid
color White
InChIInChI=1S/C8H9ClO/c9-5-7-1-3-8(6-10)4-2-7/h1-4,10H,5-6H2
InChIKeyOGALXJIOJZXBBP-UHFFFAOYSA-N
SMILESC1(CO)=CC=C(CCl)C=C1
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 1759 8/PG 2
WGK Germany 3
HS Code 2906290090
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsSkin Corr. 1B
MSDS Information
4-(CHLOROMETHYL)BENZYL ALCOHOL 99 Usage And Synthesis
Uses4-(Chloromethyl)benzyl alcohol may be used in the synthesis of 4-(chloromethyl)benzyl acetate.
Application4-(Chloromethyl)benzyl alcohol 99 is mainly used as an organic synthesis intermediate in the field of pharmaceutical research and development, and can also be used in materials synthesis and fine chemicals.
General Description4-(Chloromethyl)benzyl alcohol can be synthesized from 4-(chloromethyl)benzoyl chloride.
Synthesis
4-(Chloromethyl)benzoic acid

1642-81-5

4-(CHLOROMETHYL)BENZYL ALCOHOL  99

16473-35-1

Example 1: (1) Synthesis of [4-(chloromethyl)benzyl]alcohol: To a solution of tetrahydrofuran containing 4-(chloromethyl)benzoic acid (60 mL THF), 1M borane-THF solution (90 mL) was slowly added. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, methanol (50 mL) was added to quench the reaction. Subsequently, the solvent was removed by rotary evaporator and the obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate = 4/1 to 3/1) to afford 4-(chloromethyl)benzyl alcohol (8.84 g, 96% yield) as a colorless solid.

References[1] Patent: WO2003/106403, 2003, A1. Location in patent: Page 23
[2] Patent: US5387709, 1995, A
[3] Patent: WO2015/51045, 2015, A2. Location in patent: Page/Page column 161-162
[4] Patent: US2016/215288, 2016, A1. Location in patent: Paragraph 0602; 0611
[5] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 16, p. 4481 - 4486
Tag:4-(CHLOROMETHYL)BENZYL ALCOHOL 99(16473-35-1) Related Product Information
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