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
InChI key
MJGOLNNLNQQIHR-UHFFFAOYSA-N
InChI
1S/C7H5Cl2F/c8-4-5-6(9)2-1-3-7(5)10/h1-3H,4H2
SMILES string
Fc1cccc(Cl)c1CCl
assay
98%
form
liquid
refractive index
n20/D 1.537 (lit.)
density
1.401 g/mL at 25 °C (lit.)
functional group
chloro, fluoro
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
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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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
New synthesis of a 9-substituted adenine.
Hartman GD, et al.
The Journal of Organic Chemistry, 43(5), 960-962 (1978)
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