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Merck
CN

218111

2-Chloro-6-fluorobenzyl chloride

98%

Synonym(s):

2,α-Dichloro-6-fluorotoluene

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About This Item

Linear Formula:
ClC6H3(F)CH2Cl
CAS Number:
Molecular Weight:
179.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
259-487-5
MDL number:
Assay:
98%
Form:
liquid
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assay

98%

form

liquid

refractive index

n20/D 1.537 (lit.)

density

1.401 g/mL at 25 °C (lit.)

functional group

chloro, fluoro

SMILES string

Fc1cccc(Cl)c1CCl

InChI

1S/C7H5Cl2F/c8-4-5-6(9)2-1-3-7(5)10/h1-3H,4H2

InChI key

MJGOLNNLNQQIHR-UHFFFAOYSA-N

Application

2-Chloro-6-fluorobenzyl chloride was used:
  • as alkylating reagent during the synthesis of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole
  • in the preparataion of 2-chloro-6-fluorobenzylamine, required for the synthesis of 9-substituted adenine
  • in the preparation of aprinocid via reaction with adenine


pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

200.1 °F - closed cup

flash_point_c

93.4 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter



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New synthesis of a 9-substituted adenine.
Hartman GD, et al.
The Journal of Organic Chemistry, 43(5), 960-962 (1978)
Tissue residues of arprinocid in chickens. 1. Depletion of residues in tissues of chickens fed carbon-14-labeled arprinocid.
T A Jacob et al.
Journal of agricultural and food chemistry, 30(2), 248-253 (1982-03-01)
Vera Klimesová et al.
Farmaco (Societa chimica italiana : 1989), 59(4), 279-288 (2004-04-15)
Series of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole were synthesized by alkylation of starting triazole-3-thiol with appropriately substituted benzyl halide. All members of the set were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, M. avium, and two strains



Global Trade Item Number

SKUGTIN
218111-25G04061837071508