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916766-83-1

916766-83-1 Structure

916766-83-1 Structure
IdentificationBack Directory
[Name]

3-[4-(chloromethyl)phenyl]-1-methyl-1h-pyrazole
[CAS]

916766-83-1
[Synonyms]

3-(4-(Chloromethyl)
4-(1-Methyl-1H-pyrazol-3-yl)benzyl bromide
4-(1-Methyl-1H-pyrazol-3-yl)benzyl chloride
3-[4-(chloromethyl)phenyl]-1-methylpyrazole
4-(1-Methyl-1H-pyrazol-3-yl)benzyl bromide 97%
4-(1-Methyl-1H-pyrazol-3-yl)benzyl chloride 97%
3-[4-(chloromethyl)phenyl]-1-methyl-1h-pyrazole
1H-Pyrazole, 3-[4-(chloromethyl)phenyl]-1-methyl-
3-[4-(Chloromethyl)phenyl]-1-methyl-1H-pyrazole97%
3-[4-(Chloromethyl)phenyl]-1-methyl-1H-pyrazole 97%
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C11H11ClN2
[MDL Number]

MFCD09702351
[MOL File]

916766-83-1.mol
[Molecular Weight]

206.68
Chemical PropertiesBack Directory
[Melting point ]

78 °C
[Boiling point ]

343.3±30.0 °C(Predicted)
[density ]

1.17±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

powder
[pka]

1.53±0.10(Predicted)
[color ]

White
[Sensitive ]

Lachrymatory
[InChI]

InChI=1S/C11H11ClN2/c1-14-7-6-11(13-14)10-4-2-9(8-12)3-5-10/h2-7H,8H2,1H3
[InChIKey]

YLJMPTWMRVXTQQ-UHFFFAOYSA-N
[SMILES]

N1(C)C=CC(C2=CC=C(CCl)C=C2)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H314-H318
[Precautionary statements ]

P280-P301+P312-P303+P361+P353-P304+P340-P305+P351+P338-P310
[Hazard Codes ]

C
[Hazard Note ]

Corrosive/Lachrymatory
[HS Code ]

2933199090
Hazard InformationBack Directory
[Synthesis]

[4-(1-Methyl-1H-pyrazol-3-yl)phenyl]methanol

179055-20-0

3-[4-(chloromethyl)phenyl]-1-methyl-1h-pyrazole

916766-83-1

(C) Synthesis of 3-(4-(chloromethyl)phenyl)-1-methyl-1H-pyrazole: [4-(1-methyl-1H-pyrazol-3-yl)phenyl]methanol (1.00 g) was dissolved in THF (15.0 mL), and thionyl chloride (0.58 mL) was added slowly and dropwise under cooling in an ice bath. The reaction mixture was stirred at 17 °C for 16 hours. After the reaction was completed, it was diluted with water and ethyl acetate and neutralized by adding saturated aqueous sodium bicarbonate. The organic layer was separated, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford the target product 3-(4-(chloromethyl)phenyl)-1-methyl-1H-pyrazole (0.65 g). NMR (300 MHz, CDCl3) δ 3.95 (3H, s), 4.61 (2H, s), 6.49-6.57 (1H, m). 7.33-7.44 (3H, m), 7.74-7.82 (2H, m).

[References]

[1] Journal of Medicinal Chemistry, 2018, vol. 61, # 7, p. 2875 - 2894
[2] Patent: WO2015/163485, 2015, A1. Location in patent: Paragraph 0427
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