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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
liquid
refractive index
n20/D 1.537 (lit.)
density
1.401 g/mL at 25 °C (lit.)
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
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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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
200.1 °F
Flash Point(C)
93.4 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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)
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
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)
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